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rs1136691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1136691(C;C)
Make rs1136691(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943002
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1136691
ebirs1136691
HLIrs1136691
Exacrs1136691
Varsomers1136691
Maprs1136691
PheGenIrs1136691
hapmaprs1136691
1000 genomesrs1136691
hgdprs1136691
ensemblrs1136691
gopubmedrs1136691
geneviewrs1136691
scholarrs1136691
googlers1136691
pharmgkbrs1136691
gwascentralrs1136691
openSNPrs1136691
23andMers1136691
23andMe allrs1136691
SNP Nexus

SNPshotrs1136691
SNPdbers1136691
MSV3drs1136691
GWAS Ctlgrs1136691
Max Magnitude0
ClinVar
Risk rs1136691(A,C;A,C)
Alt rs1136691(A,C;A,C)
Reference rs1136691(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910779G>A; NC_000006.11:g.29910779G>C
CLNSRC
CLNACC