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rs61754361

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61754361(-;-)
Make rs61754361(-;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position89178521
GeneTYR
is asnp
is mentioned by
dbSNPrs61754361
ebirs61754361
HLIrs61754361
Exacrs61754361
Varsomers61754361
Maprs61754361
PheGenIrs61754361
hapmaprs61754361
1000 genomesrs61754361
hgdprs61754361
ensemblrs61754361
gopubmedrs61754361
geneviewrs61754361
scholarrs61754361
googlers61754361
pharmgkbrs61754361
gwascentralrs61754361
openSNPrs61754361
23andMers61754361
23andMe allrs61754361
SNP Nexus

SNPshotrs61754361
SNPdbers61754361
MSV3drs61754361
GWAS Ctlgrs61754361
Max Magnitude0
OMIM606933
Desc
Variant0015
Relatedalso


ClinVar
Risk rs61754361(;)
Alt rs61754361(;)
Reference rs61754361(G;G)
Significance Pathogenic
Disease Tyrosinase-negative oculocutaneous albinism not provided
Variation info
Gene TYR
CLNDBN Tyrosinase-negative oculocutaneous albinism not provided
Reversed 0
HGVS NC_000011.9:g.88911693delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000003988.2, RCV000085954.1,