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rs61760923

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61760923(C;T)
Make rs61760923(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944257
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61760923
ebirs61760923
HLIrs61760923
Exacrs61760923
Varsomers61760923
Maprs61760923
PheGenIrs61760923
hapmaprs61760923
1000 genomesrs61760923
hgdprs61760923
ensemblrs61760923
gopubmedrs61760923
geneviewrs61760923
scholarrs61760923
googlers61760923
pharmgkbrs61760923
gwascentralrs61760923
openSNPrs61760923
23andMers61760923
23andMe allrs61760923
SNP Nexus

SNPshotrs61760923
SNPdbers61760923
MSV3drs61760923
GWAS Ctlgrs61760923
Max Magnitude0
ClinVar
Risk rs61760923(T;T)
Alt rs61760923(T;T)
Reference rs61760923(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912034C>T
CLNSRC
CLNACC