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rs9260122

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9260122(G;T)
Make rs9260122(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942642
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260122
ebirs9260122
HLIrs9260122
Exacrs9260122
Varsomers9260122
Maprs9260122
PheGenIrs9260122
hapmaprs9260122
1000 genomesrs9260122
hgdprs9260122
ensemblrs9260122
gopubmedrs9260122
geneviewrs9260122
scholarrs9260122
googlers9260122
pharmgkbrs9260122
gwascentralrs9260122
openSNPrs9260122
23andMers9260122
23andMe allrs9260122
SNP Nexus

SNPshotrs9260122
SNPdbers9260122
MSV3drs9260122
GWAS Ctlgrs9260122
GMAF0.1331
Max Magnitude0
ClinVar
Risk rs9260122(T;T)
Alt rs9260122(T;T)
Reference rs9260122(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910419G>T
CLNSRC
CLNACC