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rs2507989

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2507989(G;G)
Make rs2507989(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356638
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2507989
ebirs2507989
HLIrs2507989
Exacrs2507989
Varsomers2507989
Maprs2507989
PheGenIrs2507989
hapmaprs2507989
1000 genomesrs2507989
hgdprs2507989
ensemblrs2507989
gopubmedrs2507989
geneviewrs2507989
scholarrs2507989
googlers2507989
pharmgkbrs2507989
gwascentralrs2507989
openSNPrs2507989
23andMers2507989
23andMe allrs2507989
SNP Nexus

SNPshotrs2507989
SNPdbers2507989
MSV3drs2507989
GWAS Ctlgrs2507989
GMAF0.135
Max Magnitude0
ClinVar
Risk rs2507989(G;G)
Alt rs2507989(G;G)
Reference rs2507989(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324415A>C
CLNSRC
CLNACC