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rs2308590

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2308590(A;A)
Make rs2308590(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271165
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2308590
ebirs2308590
HLIrs2308590
Exacrs2308590
Varsomers2308590
Maprs2308590
PheGenIrs2308590
hapmaprs2308590
1000 genomesrs2308590
hgdprs2308590
ensemblrs2308590
gopubmedrs2308590
geneviewrs2308590
scholarrs2308590
googlers2308590
pharmgkbrs2308590
gwascentralrs2308590
openSNPrs2308590
23andMers2308590
23andMe allrs2308590
SNP Nexus

SNPshotrs2308590
SNPdbers2308590
MSV3drs2308590
GWAS Ctlgrs2308590
GMAF0.4389
Max Magnitude0
ClinVar
Risk rs2308590(A,G,T;A,G,T)
Alt rs2308590(A,G,T;A,G,T)
Reference rs2308590(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238942G>A; NC_000006.11:g.31238942G>C; NC_000006.11:g.31238942G>T
CLNSRC
CLNACC