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rs11539957

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11539957(C;T)
Make rs11539957(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942897
GeneHLA-A
is asnp
is mentioned by
dbSNPrs11539957
ebirs11539957
HLIrs11539957
Exacrs11539957
Varsomers11539957
Maprs11539957
PheGenIrs11539957
hapmaprs11539957
1000 genomesrs11539957
hgdprs11539957
ensemblrs11539957
gopubmedrs11539957
geneviewrs11539957
scholarrs11539957
googlers11539957
pharmgkbrs11539957
gwascentralrs11539957
openSNPrs11539957
23andMers11539957
23andMe allrs11539957
SNP Nexus

SNPshotrs11539957
SNPdbers11539957
MSV3drs11539957
GWAS Ctlgrs11539957
Max Magnitude0
ClinVar
Risk rs11539957(G,T;G,T)
Alt rs11539957(G,T;G,T)
Reference rs11539957(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910674C>T
CLNSRC
CLNACC