Have questions? Visit https://www.reddit.com/r/SNPedia

rs9260186

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs9260186(C;C)
Make rs9260186(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944431
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260186
ebirs9260186
HLIrs9260186
Exacrs9260186
Varsomers9260186
Maprs9260186
PheGenIrs9260186
hapmaprs9260186
1000 genomesrs9260186
hgdprs9260186
ensemblrs9260186
gopubmedrs9260186
geneviewrs9260186
scholarrs9260186
googlers9260186
pharmgkbrs9260186
gwascentralrs9260186
openSNPrs9260186
23andMers9260186
23andMe allrs9260186
SNP Nexus

SNPshotrs9260186
SNPdbers9260186
MSV3drs9260186
GWAS Ctlgrs9260186
GMAF0.03765
Max Magnitude0
ClinVar
Risk rs9260186(C;C)
Alt rs9260186(C;C)
Reference rs9260186(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912208G>C
CLNSRC
CLNACC