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rs61760922

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61760922(A;A)
Make rs61760922(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944201
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61760922
ebirs61760922
HLIrs61760922
Exacrs61760922
Varsomers61760922
Maprs61760922
PheGenIrs61760922
hapmaprs61760922
1000 genomesrs61760922
hgdprs61760922
ensemblrs61760922
gopubmedrs61760922
geneviewrs61760922
scholarrs61760922
googlers61760922
pharmgkbrs61760922
gwascentralrs61760922
openSNPrs61760922
23andMers61760922
23andMe allrs61760922
SNP Nexus

SNPshotrs61760922
SNPdbers61760922
MSV3drs61760922
GWAS Ctlgrs61760922
Max Magnitude0
ClinVar
Risk rs61760922(A,T;A,T)
Alt rs61760922(A,T;A,T)
Reference rs61760922(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911978C>A; NC_000006.11:g.29911978C>T
CLNSRC
CLNACC