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rs1140546

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(T;T) 0 common in clinvar
Make rs1140546(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355111
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1140546
ebirs1140546
HLIrs1140546
Exacrs1140546
Varsomers1140546
Maprs1140546
PheGenIrs1140546
hapmaprs1140546
1000 genomesrs1140546
hgdprs1140546
ensemblrs1140546
gopubmedrs1140546
geneviewrs1140546
scholarrs1140546
googlers1140546
pharmgkbrs1140546
gwascentralrs1140546
openSNPrs1140546
23andMers1140546
23andMe allrs1140546
SNP Nexus

SNPshotrs1140546
SNPdbers1140546
MSV3drs1140546
GWAS Ctlgrs1140546
GMAF0.2153
Max Magnitude0
ClinVar
Risk rs1140546(C,G;C,G)
Alt rs1140546(C,G;C,G)
Reference rs1140546(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322888A>G
CLNSRC
CLNACC