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rs2507991

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2507991(G;G)
Make rs2507991(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354736
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2507991
ebirs2507991
HLIrs2507991
Exacrs2507991
Varsomers2507991
Maprs2507991
PheGenIrs2507991
hapmaprs2507991
1000 genomesrs2507991
hgdprs2507991
ensemblrs2507991
gopubmedrs2507991
geneviewrs2507991
scholarrs2507991
googlers2507991
pharmgkbrs2507991
gwascentralrs2507991
openSNPrs2507991
23andMers2507991
23andMe allrs2507991
SNP Nexus

SNPshotrs2507991
SNPdbers2507991
MSV3drs2507991
GWAS Ctlgrs2507991
GMAF0.2612
Max Magnitude0
ClinVar
Risk rs2507991(C,G;C,G)
Alt rs2507991(C,G;C,G)
Reference rs2507991(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322513A>C
CLNSRC
CLNACC