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rs9260199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9260199(A;A)
Make rs9260199(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944729
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260199
ebirs9260199
HLIrs9260199
Exacrs9260199
Varsomers9260199
Maprs9260199
PheGenIrs9260199
hapmaprs9260199
1000 genomesrs9260199
hgdprs9260199
ensemblrs9260199
gopubmedrs9260199
geneviewrs9260199
scholarrs9260199
googlers9260199
pharmgkbrs9260199
gwascentralrs9260199
openSNPrs9260199
23andMers9260199
23andMe allrs9260199
SNP Nexus

SNPshotrs9260199
SNPdbers9260199
MSV3drs9260199
GWAS Ctlgrs9260199
GMAF0.05464
Max Magnitude0
ClinVar
Risk rs9260199(A;A)
Alt rs9260199(A;A)
Reference rs9260199(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912506G>A
CLNSRC
CLNACC