Have questions? Visit https://www.reddit.com/r/SNPedia

rs11539961

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11539961(A;A)
Make rs11539961(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942876
GeneHLA-A
is asnp
is mentioned by
dbSNPrs11539961
ebirs11539961
HLIrs11539961
Exacrs11539961
Varsomers11539961
Maprs11539961
PheGenIrs11539961
hapmaprs11539961
1000 genomesrs11539961
hgdprs11539961
ensemblrs11539961
gopubmedrs11539961
geneviewrs11539961
scholarrs11539961
googlers11539961
pharmgkbrs11539961
gwascentralrs11539961
openSNPrs11539961
23andMers11539961
23andMe allrs11539961
SNP Nexus

SNPshotrs11539961
SNPdbers11539961
MSV3drs11539961
GWAS Ctlgrs11539961
Max Magnitude0
ClinVar
Risk rs11539961(A,C,T;A,C,T)
Alt rs11539961(A,C,T;A,C,T)
Reference rs11539961(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910653G>A; NC_000006.11:g.29910653G>C; NC_000006.11:g.29910653G>T
CLNSRC
CLNACC