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rs9260191

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9260191(A;G)
Make rs9260191(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944621
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260191
dbSNP (old)rs9260191
ClinGenrs9260191
ebirs9260191
HLIrs9260191
Exacrs9260191
Gnomadrs9260191
Varsomers9260191
Maprs9260191
PheGenIrs9260191
Biobankrs9260191
1000 genomesrs9260191
hgdprs9260191
ensemblrs9260191
gopubmedrs9260191
geneviewrs9260191
scholarrs9260191
googlers9260191
pharmgkbrs9260191
gwascentralrs9260191
openSNPrs9260191
23andMers9260191
23andMe allrs9260191
SNP Nexus

SNPshotrs9260191
SNPdbers9260191
MSV3drs9260191
GWAS Ctlgrs9260191
Merged fromRs113824204
GMAF0.4867
Max Magnitude0
ClinVar
Risk rs9260191(G;G) rs9260191(T;T)
Alt rs9260191(G;G) rs9260191(T;T)
Reference Rs9260191(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912398A>G
CLNSRC
CLNACC