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rs72558147

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72558147(A;A)
Make rs72558147(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271265
GeneHLA-C
is asnp
is mentioned by
dbSNPrs72558147
ebirs72558147
HLIrs72558147
Exacrs72558147
Varsomers72558147
Maprs72558147
PheGenIrs72558147
hapmaprs72558147
1000 genomesrs72558147
hgdprs72558147
ensemblrs72558147
gopubmedrs72558147
geneviewrs72558147
scholarrs72558147
googlers72558147
pharmgkbrs72558147
gwascentralrs72558147
openSNPrs72558147
23andMers72558147
23andMe allrs72558147
SNP Nexus

SNPshotrs72558147
SNPdbers72558147
MSV3drs72558147
GWAS Ctlgrs72558147
Max Magnitude0
ClinVar
Risk rs72558147(A,C,T;A,C,T)
Alt rs72558147(A,C,T;A,C,T)
Reference rs72558147(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239042C>A; NC_000006.11:g.31239042C>G; NC_000006.11:g.31239042C>T
CLNSRC
CLNACC