Have questions? Visit https://www.reddit.com/r/SNPedia

rs9260146

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9260146(C;T)
Make rs9260146(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943133
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260146
dbSNP (classic)rs9260146
ClinGenrs9260146
ebirs9260146
HLIrs9260146
Exacrs9260146
Gnomadrs9260146
Varsomers9260146
LitVarrs9260146
Maprs9260146
PheGenIrs9260146
Biobankrs9260146
1000 genomesrs9260146
hgdprs9260146
ensemblrs9260146
geneviewrs9260146
scholarrs9260146
googlers9260146
pharmgkbrs9260146
gwascentralrs9260146
openSNPrs9260146
23andMers9260146
SNPshotrs9260146
SNPdbers9260146
MSV3drs9260146
GWAS Ctlgrs9260146
GMAF0.07943
Max Magnitude0
ClinVar
Risk rs9260146(T;T)
Alt rs9260146(T;T)
Reference Rs9260146(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910910C; NC_000006.11:g.29910910C>T
CLNSRC
CLNACC