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rs61754371

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61754371(C;G)
Make rs61754371(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position89191199
GeneTYR
is asnp
is mentioned by
dbSNPrs61754371
ebirs61754371
HLIrs61754371
Exacrs61754371
Varsomers61754371
Maprs61754371
PheGenIrs61754371
hapmaprs61754371
1000 genomesrs61754371
hgdprs61754371
ensemblrs61754371
gopubmedrs61754371
geneviewrs61754371
scholarrs61754371
googlers61754371
pharmgkbrs61754371
gwascentralrs61754371
openSNPrs61754371
23andMers61754371
23andMe allrs61754371
SNP Nexus

SNPshotrs61754371
SNPdbers61754371
MSV3drs61754371
GWAS Ctlgrs61754371
Max Magnitude0
ClinVar
Risk rs61754371(G;G)
Alt rs61754371(G;G)
Reference rs61754371(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.88924367C>G
CLNSRC
CLNACC RCV000085972.1, RCV000194448.1,