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rs2308622

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2308622(A;G)
Make rs2308622(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270252
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2308622
ebirs2308622
HLIrs2308622
Exacrs2308622
Varsomers2308622
Maprs2308622
PheGenIrs2308622
hapmaprs2308622
1000 genomesrs2308622
hgdprs2308622
ensemblrs2308622
gopubmedrs2308622
geneviewrs2308622
scholarrs2308622
googlers2308622
pharmgkbrs2308622
gwascentralrs2308622
openSNPrs2308622
23andMers2308622
23andMe allrs2308622
SNP Nexus

SNPshotrs2308622
SNPdbers2308622
MSV3drs2308622
GWAS Ctlgrs2308622
GMAF0.3246
Max Magnitude0
ClinVar
Risk rs2308622(G;G)
Alt rs2308622(G;G)
Reference rs2308622(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238029T>C
CLNSRC
CLNACC