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rs72558146

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558146(C;C)
Make rs72558146(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271358
GeneHLA-C
is asnp
is mentioned by
dbSNPrs72558146
dbSNP (classic)rs72558146
ClinGenrs72558146
ebirs72558146
HLIrs72558146
Exacrs72558146
Gnomadrs72558146
Varsomers72558146
LitVarrs72558146
Maprs72558146
PheGenIrs72558146
Biobankrs72558146
1000 genomesrs72558146
hgdprs72558146
ensemblrs72558146
geneviewrs72558146
scholarrs72558146
googlers72558146
pharmgkbrs72558146
gwascentralrs72558146
openSNPrs72558146
23andMers72558146
SNPshotrs72558146
SNPdbers72558146
MSV3drs72558146
GWAS Ctlgrs72558146
Max Magnitude0
ClinVar
Risk rs72558146(C;C) rs72558146(T;T)
Alt rs72558146(C;C) rs72558146(T;T)
Reference Rs72558146(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239135C>G
CLNSRC
CLNACC