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rs1131170

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1131170(G;G)
Make rs1131170(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356928
GeneHLA-B
is asnp
is mentioned by
dbSNPrs1131170
ebirs1131170
HLIrs1131170
Exacrs1131170
Varsomers1131170
Maprs1131170
PheGenIrs1131170
hapmaprs1131170
1000 genomesrs1131170
hgdprs1131170
ensemblrs1131170
gopubmedrs1131170
geneviewrs1131170
scholarrs1131170
googlers1131170
pharmgkbrs1131170
gwascentralrs1131170
openSNPrs1131170
23andMers1131170
23andMe allrs1131170
SNP Nexus

SNPshotrs1131170
SNPdbers1131170
MSV3drs1131170
GWAS Ctlgrs1131170
GMAF0.3535
Max Magnitude0
ClinVar
Risk rs1131170(A,G;A,G)
Alt rs1131170(A,G;A,G)
Reference rs1131170(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324705A>C; NC_000006.11:g.31324705A>T
CLNSRC
CLNACC