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rs9260197

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9260197(A;G)
Make rs9260197(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944700
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260197
ebirs9260197
HLIrs9260197
Exacrs9260197
Varsomers9260197
Maprs9260197
PheGenIrs9260197
hapmaprs9260197
1000 genomesrs9260197
hgdprs9260197
ensemblrs9260197
gopubmedrs9260197
geneviewrs9260197
scholarrs9260197
googlers9260197
pharmgkbrs9260197
gwascentralrs9260197
openSNPrs9260197
23andMers9260197
23andMe allrs9260197
SNP Nexus

SNPshotrs9260197
SNPdbers9260197
MSV3drs9260197
GWAS Ctlgrs9260197
GMAF0.4894
Max Magnitude0
ClinVar
Risk rs9260197(G;G)
Alt rs9260197(G;G)
Reference rs9260197(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912477A>G
CLNSRC
CLNACC