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rs72558162

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558162(A;A)
Make rs72558162(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269580
GeneHLA-C
is asnp
is mentioned by
dbSNPrs72558162
ebirs72558162
HLIrs72558162
Exacrs72558162
Varsomers72558162
Maprs72558162
PheGenIrs72558162
hapmaprs72558162
1000 genomesrs72558162
hgdprs72558162
ensemblrs72558162
gopubmedrs72558162
geneviewrs72558162
scholarrs72558162
googlers72558162
pharmgkbrs72558162
gwascentralrs72558162
openSNPrs72558162
23andMers72558162
23andMe allrs72558162
SNP Nexus

SNPshotrs72558162
SNPdbers72558162
MSV3drs72558162
GWAS Ctlgrs72558162
Max Magnitude0
ClinVar
Risk rs72558162(A;A)
Alt rs72558162(A;A)
Reference rs72558162(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237357C>T
CLNSRC
CLNACC