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rs9260139

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9260139(C;C)
Make rs9260139(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942997
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260139
ebirs9260139
HLIrs9260139
Exacrs9260139
Varsomers9260139
Maprs9260139
PheGenIrs9260139
hapmaprs9260139
1000 genomesrs9260139
hgdprs9260139
ensemblrs9260139
gopubmedrs9260139
geneviewrs9260139
scholarrs9260139
googlers9260139
pharmgkbrs9260139
gwascentralrs9260139
openSNPrs9260139
23andMers9260139
23andMe allrs9260139
SNP Nexus

SNPshotrs9260139
SNPdbers9260139
MSV3drs9260139
GWAS Ctlgrs9260139
Max Magnitude0
ClinVar
Risk rs9260139(C;C)
Alt rs9260139(C;C)
Reference rs9260139(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910774T>C
CLNSRC
CLNACC