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rs11539964

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11539964(G;T)
Make rs11539964(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943354
GeneHLA-A
is asnp
is mentioned by
dbSNPrs11539964
ebirs11539964
HLIrs11539964
Exacrs11539964
Varsomers11539964
Maprs11539964
PheGenIrs11539964
hapmaprs11539964
1000 genomesrs11539964
hgdprs11539964
ensemblrs11539964
gopubmedrs11539964
geneviewrs11539964
scholarrs11539964
googlers11539964
pharmgkbrs11539964
gwascentralrs11539964
openSNPrs11539964
23andMers11539964
23andMe allrs11539964
SNP Nexus

SNPshotrs11539964
SNPdbers11539964
MSV3drs11539964
GWAS Ctlgrs11539964
Max Magnitude0
ClinVar
Risk rs11539964(A,C,T;A,C,T)
Alt rs11539964(A,C,T;A,C,T)
Reference rs11539964(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911131G>A; NC_000006.11:g.29911131G>C; NC_000006.11:g.29911131G>T
CLNSRC
CLNACC