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rs9260166

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9260166(C;C)
Make rs9260166(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944013
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260166
ebirs9260166
HLIrs9260166
Exacrs9260166
Varsomers9260166
Maprs9260166
PheGenIrs9260166
hapmaprs9260166
1000 genomesrs9260166
hgdprs9260166
ensemblrs9260166
gopubmedrs9260166
geneviewrs9260166
scholarrs9260166
googlers9260166
pharmgkbrs9260166
gwascentralrs9260166
openSNPrs9260166
23andMers9260166
23andMe allrs9260166
SNP Nexus

SNPshotrs9260166
SNPdbers9260166
MSV3drs9260166
GWAS Ctlgrs9260166
Max Magnitude0
ClinVar
Risk rs9260166(C;C)
Alt rs9260166(C;C)
Reference rs9260166(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911790T>C
CLNSRC
CLNACC