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rs2394961

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2394961(C;T)
Make rs2394961(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269250
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2394961
ebirs2394961
HLIrs2394961
Exacrs2394961
Varsomers2394961
Maprs2394961
PheGenIrs2394961
hapmaprs2394961
1000 genomesrs2394961
hgdprs2394961
ensemblrs2394961
gopubmedrs2394961
geneviewrs2394961
scholarrs2394961
googlers2394961
pharmgkbrs2394961
gwascentralrs2394961
openSNPrs2394961
23andMers2394961
23andMe allrs2394961
SNP Nexus

SNPshotrs2394961
SNPdbers2394961
MSV3drs2394961
GWAS Ctlgrs2394961
GMAF0.2498
Max Magnitude0
ClinVar
Risk rs2394961(T;T)
Alt rs2394961(T;T)
Reference rs2394961(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237027C>T
CLNSRC
CLNACC