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rs11757919

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11757919(A;A)
Make rs11757919(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270069
GeneHLA-C
is asnp
is mentioned by
dbSNPrs11757919
ebirs11757919
HLIrs11757919
Exacrs11757919
Varsomers11757919
Maprs11757919
PheGenIrs11757919
hapmaprs11757919
1000 genomesrs11757919
hgdprs11757919
ensemblrs11757919
gopubmedrs11757919
geneviewrs11757919
scholarrs11757919
googlers11757919
pharmgkbrs11757919
gwascentralrs11757919
openSNPrs11757919
23andMers11757919
23andMe allrs11757919
SNP Nexus

SNPshotrs11757919
SNPdbers11757919
MSV3drs11757919
GWAS Ctlgrs11757919
GMAF0.009642
Max Magnitude0
ClinVar
Risk rs11757919(A;A)
Alt rs11757919(A;A)
Reference rs11757919(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237846G>A
CLNSRC
CLNACC