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rs2507992

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2507992(A;G)
Make rs2507992(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354682
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2507992
ebirs2507992
HLIrs2507992
Exacrs2507992
Varsomers2507992
Maprs2507992
PheGenIrs2507992
hapmaprs2507992
1000 genomesrs2507992
hgdprs2507992
ensemblrs2507992
gopubmedrs2507992
geneviewrs2507992
scholarrs2507992
googlers2507992
pharmgkbrs2507992
gwascentralrs2507992
openSNPrs2507992
23andMers2507992
23andMe allrs2507992
SNP Nexus

SNPshotrs2507992
SNPdbers2507992
MSV3drs2507992
GWAS Ctlgrs2507992
GMAF0.2163
Max Magnitude0
ClinVar
Risk rs2507992(G;G)
Alt rs2507992(G;G)
Reference Rs2507992(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322459T>C
CLNSRC
CLNACC