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rs9260147

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9260147(A;A)
Make rs9260147(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943146
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260147
dbSNP (classic)rs9260147
ClinGenrs9260147
ebirs9260147
HLIrs9260147
Exacrs9260147
Gnomadrs9260147
Varsomers9260147
LitVarrs9260147
Maprs9260147
PheGenIrs9260147
Biobankrs9260147
1000 genomesrs9260147
hgdprs9260147
ensemblrs9260147
geneviewrs9260147
scholarrs9260147
googlers9260147
pharmgkbrs9260147
gwascentralrs9260147
openSNPrs9260147
23andMers9260147
SNPshotrs9260147
SNPdbers9260147
MSV3drs9260147
GWAS Ctlgrs9260147
GMAF0.1267
Max Magnitude0
ClinVar
Risk rs9260147(A;A) rs9260147(T;T)
Alt rs9260147(A;A) rs9260147(T;T)
Reference Rs9260147(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910923C; NC_000006.11:g.29910923C>A; NC_000006.11:g.29910923C>T
CLNSRC
CLNACC