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rs61760920

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61760920(C;G)
Make rs61760920(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943500
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61760920
ebirs61760920
HLIrs61760920
Exacrs61760920
Varsomers61760920
Maprs61760920
PheGenIrs61760920
hapmaprs61760920
1000 genomesrs61760920
hgdprs61760920
ensemblrs61760920
gopubmedrs61760920
geneviewrs61760920
scholarrs61760920
googlers61760920
pharmgkbrs61760920
gwascentralrs61760920
openSNPrs61760920
23andMers61760920
23andMe allrs61760920
SNP Nexus

SNPshotrs61760920
SNPdbers61760920
MSV3drs61760920
GWAS Ctlgrs61760920
Max Magnitude0
ClinVar
Risk rs61760920(G,T;G,T)
Alt rs61760920(G,T;G,T)
Reference rs61760920(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911277C>G; NC_000006.11:g.29911277C>T
CLNSRC
CLNACC