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rs2442717

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
(G;G) 0 common in clinvar
Make rs2442717(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354693
GeneHLA-B
is asnp
is mentioned by
dbSNPrs2442717
ebirs2442717
HLIrs2442717
Exacrs2442717
Varsomers2442717
Maprs2442717
PheGenIrs2442717
hapmaprs2442717
1000 genomesrs2442717
hgdprs2442717
ensemblrs2442717
gopubmedrs2442717
geneviewrs2442717
scholarrs2442717
googlers2442717
pharmgkbrs2442717
gwascentralrs2442717
openSNPrs2442717
23andMers2442717
23andMe allrs2442717
SNP Nexus

SNPshotrs2442717
SNPdbers2442717
MSV3drs2442717
GWAS Ctlgrs2442717
GMAF0.1538
Max Magnitude0
ClinVar
Risk rs2442717(C;C)
Alt rs2442717(C;C)
Reference rs2442717(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322470C>G
CLNSRC
CLNACC