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rs9260149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9260149(C;C)
Make rs9260149(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943242
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260149
ebirs9260149
HLIrs9260149
Exacrs9260149
Varsomers9260149
Maprs9260149
PheGenIrs9260149
hapmaprs9260149
1000 genomesrs9260149
hgdprs9260149
ensemblrs9260149
gopubmedrs9260149
geneviewrs9260149
scholarrs9260149
googlers9260149
pharmgkbrs9260149
gwascentralrs9260149
openSNPrs9260149
23andMers9260149
23andMe allrs9260149
SNP Nexus

SNPshotrs9260149
SNPdbers9260149
MSV3drs9260149
GWAS Ctlgrs9260149
GMAF0.3384
Max Magnitude0
ClinVar
Risk rs9260149(C;C)
Alt rs9260149(C;C)
Reference rs9260149(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911019T>C
CLNSRC
CLNACC