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rs61754365

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61754365(A;A)
Make rs61754365(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position89178603
GeneTYR
is asnp
is mentioned by
dbSNPrs61754365
ebirs61754365
HLIrs61754365
Exacrs61754365
Varsomers61754365
Maprs61754365
PheGenIrs61754365
hapmaprs61754365
1000 genomesrs61754365
hgdprs61754365
ensemblrs61754365
gopubmedrs61754365
geneviewrs61754365
scholarrs61754365
googlers61754365
pharmgkbrs61754365
gwascentralrs61754365
openSNPrs61754365
23andMers61754365
23andMe allrs61754365
SNP Nexus

SNPshotrs61754365
SNPdbers61754365
MSV3drs61754365
GWAS Ctlgrs61754365
Max Magnitude0
ClinVar
Risk rs61754365(A,T;A,T)
Alt rs61754365(A,T;A,T)
Reference rs61754365(G;G)
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.88911771G>A
CLNSRC
CLNACC RCV000085964.1, RCV000194283.1,