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rs2428496

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
(G;G) 0 common in clinvar
Make rs2428496(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354344
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2428496
ebirs2428496
HLIrs2428496
Exacrs2428496
Varsomers2428496
Maprs2428496
PheGenIrs2428496
hapmaprs2428496
1000 genomesrs2428496
hgdprs2428496
ensemblrs2428496
gopubmedrs2428496
geneviewrs2428496
scholarrs2428496
googlers2428496
pharmgkbrs2428496
gwascentralrs2428496
openSNPrs2428496
23andMers2428496
23andMe allrs2428496
SNP Nexus

SNPshotrs2428496
SNPdbers2428496
MSV3drs2428496
GWAS Ctlgrs2428496
GMAF0.1841
Max Magnitude0
ClinVar
Risk rs2428496(A;A)
Alt rs2428496(A;A)
Reference rs2428496(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322121C>T
CLNSRC
CLNACC