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rs1136656

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1136656(A;A)
Make rs1136656(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942625
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136656
ebirs1136656
HLIrs1136656
Exacrs1136656
Varsomers1136656
Maprs1136656
PheGenIrs1136656
hapmaprs1136656
1000 genomesrs1136656
hgdprs1136656
ensemblrs1136656
gopubmedrs1136656
geneviewrs1136656
scholarrs1136656
googlers1136656
pharmgkbrs1136656
gwascentralrs1136656
openSNPrs1136656
23andMers1136656
23andMe allrs1136656
SNP Nexus

SNPshotrs1136656
SNPdbers1136656
MSV3drs1136656
GWAS Ctlgrs1136656
GMAF0.1584
Max Magnitude0
ClinVar
Risk rs1136656(A;A)
Alt rs1136656(A;A)
Reference rs1136656(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910402G>A
CLNSRC
CLNACC