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rs9260118

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9260118(C;T)
Make rs9260118(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942399
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260118
ebirs9260118
HLIrs9260118
Exacrs9260118
Varsomers9260118
Maprs9260118
PheGenIrs9260118
hapmaprs9260118
1000 genomesrs9260118
hgdprs9260118
ensemblrs9260118
gopubmedrs9260118
geneviewrs9260118
scholarrs9260118
googlers9260118
pharmgkbrs9260118
gwascentralrs9260118
openSNPrs9260118
23andMers9260118
23andMe allrs9260118
SNP Nexus

SNPshotrs9260118
SNPdbers9260118
MSV3drs9260118
GWAS Ctlgrs9260118
GMAF0.3274
Max Magnitude0
ClinVar
Risk rs9260118(T;T)
Alt rs9260118(T;T)
Reference rs9260118(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910176C>T
CLNSRC
CLNACC