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rs2074496

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2074496(A;A)
Make rs2074496(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355219
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2074496
ebirs2074496
HLIrs2074496
Exacrs2074496
Varsomers2074496
Maprs2074496
PheGenIrs2074496
hapmaprs2074496
1000 genomesrs2074496
hgdprs2074496
ensemblrs2074496
gopubmedrs2074496
geneviewrs2074496
scholarrs2074496
googlers2074496
pharmgkbrs2074496
gwascentralrs2074496
openSNPrs2074496
23andMers2074496
23andMe allrs2074496
SNP Nexus

SNPshotrs2074496
SNPdbers2074496
MSV3drs2074496
GWAS Ctlgrs2074496
GMAF0.3724
Max Magnitude0
ClinVar
Risk rs2074496(A;A)
Alt rs2074496(A;A)
Reference rs2074496(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322996C>T
CLNSRC
CLNACC