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Labs To Love Health Tested Lab parents to lab pups
white labrador stud dog, white male labrador retriever dog
Powdered Snow at Labs To Love
Mischievous Loki CGC x Lunar Eclipse



White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality
White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality
White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality
White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality
White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality
White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality White Male Labrador Retriever Stud Dog, Standing at stud, Available to stud, quality
Need a Stud Dog?
Frozen Semen 
is available from our boys 
LIGHTNING
ARCTIC
POWDER
BUENROSTRO'S MISCHIEVOUS LOKI, CGC
Powder's Sire
OFA HIPS GOOD  LR-204852G
OFA ELBOWS NORMAL LR-EL59967M
CAER EYE NORMAL CERF LR-365906
OFA CARDIC NORMAL 
CARDIOLOGIST 
LR-CA6063
DEGENERATIVE MYELOPATHY
 DNA CLEAR/NORMAL
EXECISE INDUCED COLLAPSE
 DNA CLEAR/NORMAL
COAT COLOR DNA TEST 
DOES NOT CARRY DILUTE GENE

BUENROSTRO'S LUNAR ECLIPSE
Powder's Dam
OFA HIPS GOOD LR-206985G
OFA ELBOWS NORMAL LR-EL61674F24
CAER EYE NORMAL LR-EYE4557
PRCD DNA CLEAR/NORMAL
CENTRONUCLEAR MYOPATHY CNM CLEAR/NORMAL 
DEGENERATIVE MYELOPATHY
DNA CLEAR/NORMAL
EXECISE INDUCED COLLAPSE
DNA CLEAR/NORMAL
COAT COLOR DNA TEST 
DOES NOT CARRY DILUTE GENE

Powdered Snow at Labs To Love
OFA HIPS EXCELLENT - OFA ELBOWS NORMAL 
ACVO CLEAR / NORMAL - OFA EYE LR-EYE7855 (CAER)
OPTIGEN 1A  DNA TESTED CLEAR/NORMAL LR-PRA1272
PRCD PROGRESSIVE RETINAL ATROPHY CLEAR/NORMAL
OFA CARDIAC TESTED NORMAL LR-CA10089
EXERCISED INDUCED COLLAPSE (EIC) DNA TESTED NORMAL/CLEAR LR-EIC3230 
CENTRONUCLEAR MYOPATHY (CNM) DNA CLEAR/NORMAL LR-CNM1066
CYSTINURIA (CY) DNA CLEAR/NORMAL LY-CY61
DEGENERATIVE MYELOPATHY DNA CLEAR/NORMAL LR-DM390
HYPERURICOSURIA (HU) DNA CLEAR/NORMAL LR-HU31
AKC DNA PROFILED V770930  -   CHIC123108
 OFA FULL DENTITION - CORRECT SCISSORS BITE  LR-DE546
D LOCUS DD = DOES NOT CARRY DILUTE GENE LR-DL268

Our boy is also cleared through DNA Health testing for 171 more health tests listed below!

EYE CLEARANCES: Progressive Retinal Atrophy - PRCD1 - CLEAR/NORMAL
Progressive Retinal Atrophy - PRCD3 - CLEAR/NORMAL
Progressive Retinal Atrophy - CNGA - CLEAR/NORMAL
Progressive Retinal Atrophy - PRCD - CLEAR/NORMAL
Progressive Retinal Atrophy -  CNGB1 - CLEAR/NORMAL
Progressive Retinal Atrophy - SAG - CLEAR/NORMAL
Progressive Retinal Atrophy 1 - SLC4A3 - CLEAR/NORMAL
Progressive Retinal Atrophy 2 - TTC8 - CLEAR/NORMAL
Progressive Retinal Atrophy - CRD1 - PDE6B - CLEAR/NORMAL
Progressive Retinal Atrophy -  CRD2 -  IQCB1 - CLEAR/NORMAL
Progressive Retinal Atrophy - CRD4/CORD1 - RPGRIP1 - CLEAR/NORMAL
Choroidal Hypoplasia - NHEJ1 - CLEAR/NORMAL
Achromatopsia - CNGA3 Exon 7 - CLEAR/NORMAL
Autosomal Dominant Progressive Retinal Atrophy - CLEAR/NORMAL
Canine Multifocal Retinopathy - CMR1 - CLEAR/NORMAL
Canine Multifocal Retinopathy - CMR3 - CLEAR/NORMAL
Canine Multifocal Retinopathy - CMR3 -  BEST1 EXON 10 SNP - CLEAR/NORMAL
Glaucoma - Primary Open Angle Glaucoma - ADAMTS10 Exon 9 - CLEAR/NORMAL
Glaucoma - Primary Open Angle Glaucoma - ADAMTS10 Exon 17 - CLEAR/NORMAL
Glaucoma - Primary Open Angle Glaucoma - ADAMTS17 Exon 11 - CLEAR/NORMAL
Glaucoma - Primary Open Angle Glaucoma - ADAMTS10 Exon 2 - CLEAR/NORMAL
Hereditary Cataracts, Early Onset Cataracts, Juvenile Cataracts - CLEAR/NORMAL
Primary Lens Luxation -  CLEAR/NORMAL
Congenital Stationary Night Blindness  -  CLEAR/NORMAL
Macular Corneal Dystrophy (MCD) - CLEAR/NORMAL
CLINICAL CLEARANCES: MDR1 Drug Sensitivity - CLEAR/NORMAL
Alanine Aminotransfearase (ALT) Activity - CLEAR/NORMAL
BLOOD CLEARANCES: P2y12 Receptor Platelet Disorder -  CLEAR/NORMAL
Factor IX Deficiency, Hemophilia B - F9 Exon 7 - CLEAR/NORMAL
Factor VIII Deficiency Hemophilia A - F8 Exon 11 - CLEAR/NORMAL
Factor VIII Deficiency Hemophilia A - F8 Exon 1 - CLEAR/NORMAL
Thrombopathia Exon 5 - CLEAR/NORMAL
Thrombopathia Exon 8 - CLEAR/NORMAL
Von Willebrand Disease Type III - CLEAR/NORMAL
Von Willebrand Disease Type II - CLEAR/NORMAL
Von Willebrand Disease Type I - CLEAR/NORMAL
Canine Leukocyte Adhesion Deficienecy Type III (LAD3) - CLEAR/NORMAL
Congential Macrothrombocytopenia - CLEAR/NORMAL
Canine Elliptocytosis -  CLEAR/NORMAL
Canine Neutropenia - CLEAR/NORMAL
Glanzmann's Thrombasthenia Type I - CLEAR/NORMAL
May-Hegglin Anomaly - CLEAR/NORMAL
Prekallikrein Deficiency - CLEAR/NORMAL
Pyruvate Kinase Deficiency Exon 5 - CLEAR/NORMAL
Pyruvate Kinase Deficiency Exon 7 - CLEAR/NORMAL
Pyruvate Kinase Deficiency Exon 10 - CLEAR/NORMAL
Trapped Neutrophil Syndrome - CLEAR/NORMAL
Ligneous Membranitis - CLEAR/NORMAL 
IMMUNE CLEARANCES: Complement 3 (C3) Deficiency - CLEAR/NORMAL
Severe Combined Immunodeficiency - PRKDC - CLEAR/NORMAL
Severe Combined Immunodeficiency - RAG1 - CLEAR/NORMAL
X-Linked Severe Combined Immunodeficiency - Variant 1 - CLEAR/NORMAL
X-Linked Severe Combined Immunodeficiency - Variant 2 - CLEAR/NORMAL
HORMONE CLEARANCES: Congenital Hypothyroidism - CLEAR/NORMAL
MULTISYSTEM CLEARANCES: Glycogen Storage Disease Von Gierke Disease - CLEAR/NORMAL
Primary Ciliary Dyskinesia - CLEAR/NORMAL
Congenital Keratoconjunctivitis Sicca & Ichthyosiform Dermatosis (CKCSID) - CLEAR/NORMAL
Dry Eye Curly Coat Syndrome - CLEAR/NORMAL
X-Linked Ectodermal Dysplasia - CLEAR/NORMAL
Anhidrotic Ectodermal Dysplasia - CLEAR/NORMAL
Renal Cystadenocarcinoma & Nodular Dermatofibrosis (RCND) - CLEAR/NORMAL
Canine Fucosidosis - CLEAR/NORMAL
Glycogen Storage Disease Type II  Pompe's Disease - CLEAR/NORMAL
Glycogen Storage Disease Type IIIa (GSD IIIa) - CLEAR/NORMAL
Mucopolysaccharidosis Type I - CLEAR/NORMAL
Mucopolysaccharidosis Type IIIA Sanflilppo Syndrome Type A - Variant 1 - CLEAR/NORMAL
Mucopolysaccharidosis Type IIIA Sanflilppo Syndrome Type A - Variant 2 - CLEAR/NORMAL
Mucopolysaccharidosis Type VII Exon 3 Sly Syndrome - CLEAR/NORMAL
Mucopolysaccharidosis Type VII Exon 5 Sly Syndrome - CLEAR/NORMAL
Glycogen Storage Disease Type II Phosphofructokinase Deficiency - CLEAR/NORMAL
Lagotto Storage Disease - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 1 -  CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 2 - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 1 - Cerebellar Ataxia NCL A - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 1 - CLN5 - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 6 - CLN6 Exon 7- CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 8 - CLN8 - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis  - CLEAR/NORMAL
Neuronal Ceroid Lipofuscinosis 10 - CTSD Exon 5 - CLEAR/NORMAL
Adult Onset Neuronal Ceroid Lipofuscinosis - CLEAR/NORMAL
GM1 Gangliosidosis Exon 2 - CLEAR/NORMAL
GM1 Gangliosidosis Exon 15 - CLEAR/NORMAL
GM2 Gangliosidosis Exon 2 - CLEAR/NORMAL
GM2 Gangliosidosis Hexa - CLEAR/NORMAL
Globoid Cell Leukodystrophy, Krabbe Disease - CLEAR/NORMAL
KIDNEY & BLADDER CLEARANCES: 2, 8-Dihydroxyadenine (2,80DHA) Urolithiasis - CLEAR/NORMAL
Cystinuria Type I-A - SLC3A1 - CLEAR/NORMAL
Cystinuria Type I-A - SLC7A9 - CLEAR/NORMAL
Cystinuria Type II-A - CLEAR/NORMAL
Hyperuricosuria & Hyperuricemia or Urolithiasis - CLEAR/NORMAL
Polycystic Kidney Disease - CLEAR/NORMAL
Primary Hyperoxaluria - CLEAR/NORMAL
Protein Losing Nephropathy - CLEAR/NORMAL
X-Linked Hereditary Nephropathy (Variant 2) - CLEAR/NORMAL
Autosomal Recessive Hereditary Nephropathy (Familial Nephropathy) - CLEAR/NORMAL
OTHER HEALTH CLEARANCES: Autosomal Recessive Amelogenesis Imperfecta - CLEAR/NORMAL
Persistent Mullerian Duct Syndrome - CLEAR/NORMAL
Deafness & Vestibular Syndrome - CLEAR/NORMAL
Autoinflammatory Disease - CLEAR/NORMAL
BRAIN & SPINAL CORD CLEARANCES: Alexander Disease - CLEAR/NORMAL
Encephalopathy, Subacute Necrotizing Encephalomyelopathy -  CLEAR/NORMAL
Cerebellar Abiotrophy, Neonatal Cerebellar Cortical Degeneration - CLEAR/NORMAL
Cerebellar Ataxia, Progressive Early-Onset Cerebellar Ataxia - CLEAR/NORMAL
Cerebellar Hypoplasia - CLEAR/NORMAL
Spinocerebellar Ataxia, Late-Onset Ataxia - CLEAR/NORMAL
Spinocerebellar Ataxia with Myokymia and/or Seizures - CLEAR/NORMAL
Benign Familial Juvenile Epilepsy, Remitting Focal Epilepsy - CLEAR/NORMAL
Degenerative Myelopathy - CLEAR/NORMAL
Fetal-Onset Neonatal Neuroaxonal Dystrophy - CLEAR/NORMAL
Hypomyelination & Tremors - CLEAR/NORMAL
Shaking Puppy Syndrome, X-Linked Generalized Tremor Syndrome - CLEAR/NORMAL
L-2-Hydroxyglutaric Aciduria - CLEAR/NORMAL
Neonatal Encephalopathy with Seizures (NEWS) - CLEAR/NORMAL
Polyneuropathy, NDRG1 Exon 15 - CLEAR/NORMAL
Polyneuropathy, NDRG1 Exon 4 - CLEAR/NORMAL
Narcolepsy - CLEAR/NORMAL
Progressive Neuronal Abiotrophy (canine Multiple System Degeneration) Exon 4 - CLEAR/NORMAL
Progressive Neuronal Abiotrophy (canine Multiple System Degeneration) Exon 15 - CLEAR/NORMAL
Juvenile Laryngeal Paralysis & Polyneuropathy, Polyneuropathy with Ocular Abnormalities & Neuronal Vacuolation (POANV) - CLEAR/NORMAL 
Hereditary Sensory Autonomic Neuropathy (HSAN), Acral Mutilation Syndrome - CLEAR/NORMAL
Juvenile Onset Polyneuropathy, Leonberger Polyneuropathy 1 - CLEAR/NORMAL
Spongy Degeneration with Cerebellar Ataxia 1, SeSAME/EAST - CLEAR/NORMAL
Spongy Degeneration with Cerebellar Ataxia 2, SeSAME/EAST - CLEAR/NORMAL
HEART CLEARANCES: Dilated Cardiomyopathy -  CLEAR/NORMAL
Long QT Syndrome - CLEAR/NORMAL
MUSCULAR CLEARANCES: Muscular Dystrophy - CLEAR/NORMAL
Centronuclear Myopathy - CLEAR/NORMAL
Exercise-Induced Collapse - CLEAR/NORMAL
Inherited Myopathy - CLEAR/NORMAL
Myostatin Deficiency - CLEAR/NORMAL
Myotonia Congenita Exon 7 - CLEAR/NORMAL
Myotonia Congenita Exon 23 - CLEAR/NORMAL
Myotubular Myopathy 1, X-linked Myotubular Myopathy - CLEAR/NORMAL 
METABOLIC CLEARANCES: Hypocatalasia, Acatalasemia - CLEAR/NORMAL
Pyruvate Dehydrogenase Deficiency - CLEAR/NORMAL
Malignant Hyperthermia - CLEAR/NORMAL 
GASTROINTESTINAL CLEARANCES: 
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption Exon 8 - CLEAR/NORMAL
Imerslund-Grasbeck Syndrome, Selective Cobalamin Malabsorption Exon 53 - CLEAR/NORMAL
NEUROMUSCULAR CLEARANCES:  Congenital Myasthenic Syndrome CHAT - CLEAR/NORMAL
Congenital Myasthenic Syndrome COLQ - CLEAR/NORMAL
Episodic Falling Syndrome - CLEAR/NORMAL
SKIN & CONNECTIVE TISSUES CLEARANCES: Dystrophic Epidermolysis BUllosa - CLEAR/NORMAL
Ectodermal Dysplasia, SKin Fragility SYndrome - CLEAR/NORMAL
Ichthyosis, Epidermolytic Hyperkeratosis - CLEAR/NORMAL
Ichthyosis PNPLA1 - CLEAR/NORMAL
Ichthyosis SLC27A4 - CLEAR/NORMAL
Ichthyosis NIPAL4 - CLEAR/NORMAL
Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita - CLEAR/NORMAL
Hereditary Footpad Hyperkeratosis - CLEAR/NORMAL
Hereditary Nasal Parakeratosis HNPK - CLEAR/NORMAL
Musladin-Lueke Syndrome - CLEAR/NORMAL 
SKELETAL CLEARANCES: Cleft Lip and/or Cleft Palate - CLEAR/NORMAL 
Hereditary Vitamin D-Resistant Rickets - CLEAR/NORMAL
Oculoskeletal Dysplasia 1, Dwarfism-Retinal Dysplasia - CLEAR/NORMAL 
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A1) - CLEAR/NORMAL 
Osteogenesis Imperfecta, Brittle Bone Disease (COL1A2) - CLEAR/NORMAL 
Osteogenesis Imperfecta, Brittle Bone Disease (SERPINH1)  - CLEAR/NORMAL
Osteochondrodysplasia, Skeletal Dwarfism - CLEAR/NORMAL 
Skeletal Dysplasia 2 - CLEAR/NORMAL 
Craniomandibular Osteopathy (CMO) - CLEAR/NORMAL
COAT COLOR CLEARANCES: 
E Locus (MC1R) - No dark hairs anywhere 
D Locus (MLPH) Does not carry Dilute - CLEAR/NORMAL
B Locus  (TYRP1) Produces Black pigment in skin, noses, eye rims and footpads

We are happy to share photos of Powder's dam & sire, with permission from Amy Buenrostro LuvMyLabradors