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rs72558148

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558148(C;G)
Make rs72558148(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271213
GeneHLA-C
is asnp
is mentioned by
dbSNPrs72558148
ebirs72558148
HLIrs72558148
Exacrs72558148
Varsomers72558148
Maprs72558148
PheGenIrs72558148
hapmaprs72558148
1000 genomesrs72558148
hgdprs72558148
ensemblrs72558148
gopubmedrs72558148
geneviewrs72558148
scholarrs72558148
googlers72558148
pharmgkbrs72558148
gwascentralrs72558148
openSNPrs72558148
23andMers72558148
23andMe allrs72558148
SNP Nexus

SNPshotrs72558148
SNPdbers72558148
MSV3drs72558148
GWAS Ctlgrs72558148
Max Magnitude0
ClinVar
Risk rs72558148(G,T;G,T)
Alt rs72558148(G,T;G,T)
Reference rs72558148(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238990G>A; NC_000006.11:g.31238990G>C
CLNSRC
CLNACC