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rs2428495

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
(G;G) 0 common in clinvar
Make rs2428495(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354398
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2428495
ebirs2428495
HLIrs2428495
Exacrs2428495
Varsomers2428495
Maprs2428495
PheGenIrs2428495
hapmaprs2428495
1000 genomesrs2428495
hgdprs2428495
ensemblrs2428495
gopubmedrs2428495
geneviewrs2428495
scholarrs2428495
googlers2428495
pharmgkbrs2428495
gwascentralrs2428495
openSNPrs2428495
23andMers2428495
23andMe allrs2428495
SNP Nexus

SNPshotrs2428495
SNPdbers2428495
MSV3drs2428495
GWAS Ctlgrs2428495
GMAF0.1878
Max Magnitude0
ClinVar
Risk rs2428495(A;A)
Alt rs2428495(A;A)
Reference rs2428495(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322175C>T
CLNSRC
CLNACC