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rs9260169

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9260169(C;T)
Make rs9260169(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944059
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260169
ebirs9260169
HLIrs9260169
Exacrs9260169
Varsomers9260169
Maprs9260169
PheGenIrs9260169
hapmaprs9260169
1000 genomesrs9260169
hgdprs9260169
ensemblrs9260169
gopubmedrs9260169
geneviewrs9260169
scholarrs9260169
googlers9260169
pharmgkbrs9260169
gwascentralrs9260169
openSNPrs9260169
23andMers9260169
23andMe allrs9260169
SNP Nexus

SNPshotrs9260169
SNPdbers9260169
MSV3drs9260169
GWAS Ctlgrs9260169
GMAF0.2681
Max Magnitude0
ClinVar
Risk rs9260169(T;T)
Alt rs9260169(T;T)
Reference rs9260169(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911836C>T
CLNSRC
CLNACC