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rs1131156

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1131156(C;G)
Make rs1131156(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357118
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1131156
ebirs1131156
HLIrs1131156
Exacrs1131156
Varsomers1131156
Maprs1131156
PheGenIrs1131156
hapmaprs1131156
1000 genomesrs1131156
hgdprs1131156
ensemblrs1131156
gopubmedrs1131156
geneviewrs1131156
scholarrs1131156
googlers1131156
pharmgkbrs1131156
gwascentralrs1131156
openSNPrs1131156
23andMers1131156
23andMe allrs1131156
SNP Nexus

SNPshotrs1131156
SNPdbers1131156
MSV3drs1131156
GWAS Ctlgrs1131156
GMAF0.4908
Max Magnitude0
ClinVar
Risk rs1131156(A,G;A,G)
Alt rs1131156(A,G;A,G)
Reference rs1131156(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324895G>C; NC_000006.11:g.31324895G>T
CLNSRC
CLNACC


[PMID 18974781OA-icon.png] Cataloging coding sequence variations in human genome databases.