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rs75912596

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs75912596(A;G)
Make rs75912596(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271093
GeneHLA-C
is asnp
is mentioned by
dbSNPrs75912596
ebirs75912596
HLIrs75912596
Exacrs75912596
Varsomers75912596
Maprs75912596
PheGenIrs75912596
hapmaprs75912596
1000 genomesrs75912596
hgdprs75912596
ensemblrs75912596
gopubmedrs75912596
geneviewrs75912596
scholarrs75912596
googlers75912596
pharmgkbrs75912596
gwascentralrs75912596
openSNPrs75912596
23andMers75912596
23andMe allrs75912596
SNP Nexus

SNPshotrs75912596
SNPdbers75912596
MSV3drs75912596
GWAS Ctlgrs75912596
Max Magnitude0
ClinVar
Risk rs75912596(G;G)
Alt rs75912596(G;G)
Reference rs75912596(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238870T>C
CLNSRC
CLNACC