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rs2234776

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2234776(A;A)
Make rs2234776(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270120
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2234776
ebirs2234776
HLIrs2234776
Exacrs2234776
Varsomers2234776
Maprs2234776
PheGenIrs2234776
hapmaprs2234776
1000 genomesrs2234776
hgdprs2234776
ensemblrs2234776
gopubmedrs2234776
geneviewrs2234776
scholarrs2234776
googlers2234776
pharmgkbrs2234776
gwascentralrs2234776
openSNPrs2234776
23andMers2234776
23andMe allrs2234776
SNP Nexus

SNPshotrs2234776
SNPdbers2234776
MSV3drs2234776
GWAS Ctlgrs2234776
GMAF0.2438
Max Magnitude0
ClinVar
Risk rs2234776(A;A)
Alt rs2234776(A;A)
Reference rs2234776(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237897C>T
CLNSRC
CLNACC