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rs66459704

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs66459704(C;C)
Make rs66459704(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269660
GeneHLA-C
is asnp
is mentioned by
dbSNPrs66459704
ebirs66459704
HLIrs66459704
Exacrs66459704
Varsomers66459704
Maprs66459704
PheGenIrs66459704
hapmaprs66459704
1000 genomesrs66459704
hgdprs66459704
ensemblrs66459704
gopubmedrs66459704
geneviewrs66459704
scholarrs66459704
googlers66459704
pharmgkbrs66459704
gwascentralrs66459704
openSNPrs66459704
23andMers66459704
23andMe allrs66459704
SNP Nexus

SNPshotrs66459704
SNPdbers66459704
MSV3drs66459704
GWAS Ctlgrs66459704
GMAF0.2204
Max Magnitude0
ClinVar
Risk rs66459704(C;C)
Alt rs66459704(C;C)
Reference rs66459704(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237437T>C
CLNSRC
CLNACC