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

rs1137296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1137296(C;C)
Make rs1137296(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945075
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1137296
ebirs1137296
HLIrs1137296
Exacrs1137296
Varsomers1137296
Maprs1137296
PheGenIrs1137296
hapmaprs1137296
1000 genomesrs1137296
hgdprs1137296
ensemblrs1137296
gopubmedrs1137296
geneviewrs1137296
scholarrs1137296
googlers1137296
pharmgkbrs1137296
gwascentralrs1137296
openSNPrs1137296
23andMers1137296
23andMe allrs1137296
SNP Nexus

SNPshotrs1137296
SNPdbers1137296
MSV3drs1137296
GWAS Ctlgrs1137296
GMAF0.3485
Max Magnitude0
ClinVar
Risk rs1137296(C;C)
Alt rs1137296(C;C)
Reference rs1137296(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912852T>C
CLNSRC
CLNACC