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rs62645917

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs62645917(C;T)
Make rs62645917(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position89284792
GeneTYR
is asnp
is mentioned by
dbSNPrs62645917
ebirs62645917
HLIrs62645917
Exacrs62645917
Varsomers62645917
Maprs62645917
PheGenIrs62645917
hapmaprs62645917
1000 genomesrs62645917
hgdprs62645917
ensemblrs62645917
gopubmedrs62645917
geneviewrs62645917
scholarrs62645917
googlers62645917
pharmgkbrs62645917
gwascentralrs62645917
openSNPrs62645917
23andMers62645917
23andMe allrs62645917
SNP Nexus

SNPshotrs62645917
SNPdbers62645917
MSV3drs62645917
GWAS Ctlgrs62645917
Max Magnitude0
ClinVar
Risk rs62645917(T;T)
Alt rs62645917(T;T)
Reference rs62645917(C;C)
Significance Pathogenic
Disease not provided Tyrosinase-negative oculocutaneous albinism
Variation info
Gene TYR
CLNDBN not provided Tyrosinase-negative oculocutaneous albinism
Reversed 0
HGVS NC_000011.9:g.89017960C>T
CLNSRC
CLNACC RCV000085909.1, RCV000194121.1,