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rs9260198

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9260198(C;T)
Make rs9260198(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944725
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260198
ebirs9260198
HLIrs9260198
Exacrs9260198
Varsomers9260198
Maprs9260198
PheGenIrs9260198
hapmaprs9260198
1000 genomesrs9260198
hgdprs9260198
ensemblrs9260198
gopubmedrs9260198
geneviewrs9260198
scholarrs9260198
googlers9260198
pharmgkbrs9260198
gwascentralrs9260198
openSNPrs9260198
23andMers9260198
23andMe allrs9260198
SNP Nexus

SNPshotrs9260198
SNPdbers9260198
MSV3drs9260198
GWAS Ctlgrs9260198
Max Magnitude0
ClinVar
Risk rs9260198(T;T)
Alt rs9260198(T;T)
Reference rs9260198(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912502C>T
CLNSRC
CLNACC