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rs1140487

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1140487(A;A)
Make rs1140487(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355210
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1140487
ebirs1140487
HLIrs1140487
Exacrs1140487
Varsomers1140487
Maprs1140487
PheGenIrs1140487
hapmaprs1140487
1000 genomesrs1140487
hgdprs1140487
ensemblrs1140487
gopubmedrs1140487
geneviewrs1140487
scholarrs1140487
googlers1140487
pharmgkbrs1140487
gwascentralrs1140487
openSNPrs1140487
23andMers1140487
23andMe allrs1140487
SNP Nexus

SNPshotrs1140487
SNPdbers1140487
MSV3drs1140487
GWAS Ctlgrs1140487
GMAF0.03122
Max Magnitude0
ClinVar
Risk rs1140487(A;A)
Alt rs1140487(A;A)
Reference rs1140487(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322987C>T
CLNSRC
CLNACC