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rs9260120

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9260120(C;C)
Make rs9260120(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942500
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260120
ebirs9260120
HLIrs9260120
Exacrs9260120
Varsomers9260120
Maprs9260120
PheGenIrs9260120
hapmaprs9260120
1000 genomesrs9260120
hgdprs9260120
ensemblrs9260120
gopubmedrs9260120
geneviewrs9260120
scholarrs9260120
googlers9260120
pharmgkbrs9260120
gwascentralrs9260120
openSNPrs9260120
23andMers9260120
23andMe allrs9260120
SNP Nexus

SNPshotrs9260120
SNPdbers9260120
MSV3drs9260120
GWAS Ctlgrs9260120
GMAF0.08402
Max Magnitude0
ClinVar
Risk rs9260120(C,T;C,T)
Alt rs9260120(C,T;C,T)
Reference rs9260120(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910277G>C
CLNSRC
CLNACC