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rs150127748

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150127748(C;G)
Make rs150127748(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271120
GeneHLA-C
is asnp
is mentioned by
dbSNPrs150127748
ebirs150127748
HLIrs150127748
Exacrs150127748
Varsomers150127748
Maprs150127748
PheGenIrs150127748
hapmaprs150127748
1000 genomesrs150127748
hgdprs150127748
ensemblrs150127748
gopubmedrs150127748
geneviewrs150127748
scholarrs150127748
googlers150127748
pharmgkbrs150127748
gwascentralrs150127748
openSNPrs150127748
23andMers150127748
23andMe allrs150127748
SNP Nexus

SNPshotrs150127748
SNPdbers150127748
MSV3drs150127748
GWAS Ctlgrs150127748
Max Magnitude0
ClinVar
Risk rs150127748(G;G)
Alt rs150127748(G;G)
Reference rs150127748(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31238897C>G
CLNSRC
CLNACC