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rs2523609

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2523609(C;T)
Make rs2523609(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269478
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2523609
ebirs2523609
HLIrs2523609
Exacrs2523609
Varsomers2523609
Maprs2523609
PheGenIrs2523609
hapmaprs2523609
1000 genomesrs2523609
hgdprs2523609
ensemblrs2523609
gopubmedrs2523609
geneviewrs2523609
scholarrs2523609
googlers2523609
pharmgkbrs2523609
gwascentralrs2523609
openSNPrs2523609
23andMers2523609
23andMe allrs2523609
SNP Nexus

SNPshotrs2523609
SNPdbers2523609
MSV3drs2523609
GWAS Ctlgrs2523609
GMAF0.2548
Max Magnitude0
ClinVar
Risk rs2523609(T;T)
Alt rs2523609(T;T)
Reference rs2523609(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237255G>A
CLNSRC
CLNACC