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rs61754392

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs61754392(A;A)
Make rs61754392(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position89284843
GeneTYR
is asnp
is mentioned by
dbSNPrs61754392
ebirs61754392
HLIrs61754392
Exacrs61754392
Varsomers61754392
Maprs61754392
PheGenIrs61754392
hapmaprs61754392
1000 genomesrs61754392
hgdprs61754392
ensemblrs61754392
gopubmedrs61754392
geneviewrs61754392
scholarrs61754392
googlers61754392
pharmgkbrs61754392
gwascentralrs61754392
openSNPrs61754392
23andMers61754392
23andMe allrs61754392
SNP Nexus

SNPshotrs61754392
SNPdbers61754392
MSV3drs61754392
GWAS Ctlgrs61754392
Max Magnitude0
OMIM606933
Desc
Variant0022
Relatedalso
ClinVar
Risk rs61754392(A;A)
Alt rs61754392(A;A)
Reference rs61754392(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.89018011G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003995.2, RCV000085914.1,