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rs45481597

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45481597(C;T)
Make rs45481597(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270220
GeneHLA-C
is asnp
is mentioned by
dbSNPrs45481597
ebirs45481597
HLIrs45481597
Exacrs45481597
Varsomers45481597
Maprs45481597
PheGenIrs45481597
hapmaprs45481597
1000 genomesrs45481597
hgdprs45481597
ensemblrs45481597
gopubmedrs45481597
geneviewrs45481597
scholarrs45481597
googlers45481597
pharmgkbrs45481597
gwascentralrs45481597
openSNPrs45481597
23andMers45481597
23andMe allrs45481597
SNP Nexus

SNPshotrs45481597
SNPdbers45481597
MSV3drs45481597
GWAS Ctlgrs45481597
Max Magnitude0
ClinVar
Risk rs45481597(T;T)
Alt rs45481597(T;T)
Reference rs45481597(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237997G>A
CLNSRC
CLNACC