Have questions? Visit https://www.reddit.com/r/SNPedia

rs61754365

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61754365(A;A)
Make rs61754365(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position89178603
GeneLOC107984363, TYR
is asnp
is mentioned by
dbSNPrs61754365
dbSNP (classic)rs61754365
ClinGenrs61754365
ebirs61754365
HLIrs61754365
Exacrs61754365
Gnomadrs61754365
Varsomers61754365
LitVarrs61754365
Maprs61754365
PheGenIrs61754365
Biobankrs61754365
1000 genomesrs61754365
hgdprs61754365
ensemblrs61754365
geneviewrs61754365
scholarrs61754365
googlers61754365
pharmgkbrs61754365
gwascentralrs61754365
openSNPrs61754365
23andMers61754365
SNPshotrs61754365
SNPdbers61754365
MSV3drs61754365
GWAS Ctlgrs61754365
Max Magnitude0
ClinVar
Risk rs61754365(A;A) rs61754365(T;T)
Alt rs61754365(A;A) rs61754365(T;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 UniProtKB (protein)
CLNACC RCV000085964.1, RCV000194283.1,