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rs11539959

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11539959(C;C)
Make rs11539959(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942864
GeneHLA-A
is asnp
is mentioned by
dbSNPrs11539959
ebirs11539959
HLIrs11539959
Exacrs11539959
Varsomers11539959
Maprs11539959
PheGenIrs11539959
hapmaprs11539959
1000 genomesrs11539959
hgdprs11539959
ensemblrs11539959
gopubmedrs11539959
geneviewrs11539959
scholarrs11539959
googlers11539959
pharmgkbrs11539959
gwascentralrs11539959
openSNPrs11539959
23andMers11539959
23andMe allrs11539959
SNP Nexus

SNPshotrs11539959
SNPdbers11539959
MSV3drs11539959
GWAS Ctlgrs11539959
Max Magnitude0
ClinVar
Risk rs11539959(A,C,T;A,C,T)
Alt rs11539959(A,C,T;A,C,T)
Reference rs11539959(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910641G>A; NC_000006.11:g.29910641G>C; NC_000006.11:g.29910641G>T
CLNSRC
CLNACC