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rs9260196

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9260196(C;C)
Make rs9260196(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944696
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260196
ebirs9260196
HLIrs9260196
Exacrs9260196
Varsomers9260196
Maprs9260196
PheGenIrs9260196
hapmaprs9260196
1000 genomesrs9260196
hgdprs9260196
ensemblrs9260196
gopubmedrs9260196
geneviewrs9260196
scholarrs9260196
googlers9260196
pharmgkbrs9260196
gwascentralrs9260196
openSNPrs9260196
23andMers9260196
23andMe allrs9260196
SNP Nexus

SNPshotrs9260196
SNPdbers9260196
MSV3drs9260196
GWAS Ctlgrs9260196
GMAF0.4908
Max Magnitude0
ClinVar
Risk rs9260196(C;C)
Alt rs9260196(C;C)
Reference rs9260196(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912473T>C
CLNSRC
CLNACC