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rs9260155

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9260155(C;C)
Make rs9260155(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943462
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260155
dbSNP (classic)rs9260155
ClinGenrs9260155
ebirs9260155
HLIrs9260155
Exacrs9260155
Gnomadrs9260155
Varsomers9260155
LitVarrs9260155
Maprs9260155
PheGenIrs9260155
Biobankrs9260155
1000 genomesrs9260155
hgdprs9260155
ensemblrs9260155
geneviewrs9260155
scholarrs9260155
googlers9260155
pharmgkbrs9260155
gwascentralrs9260155
openSNPrs9260155
23andMers9260155
SNPshotrs9260155
SNPdbers9260155
MSV3drs9260155
GWAS Ctlgrs9260155
GMAF0.2888
Max Magnitude0
ClinVar
Risk rs9260155(A;A) rs9260155(C;C) rs9260155(G;G)
Alt rs9260155(A;A) rs9260155(C;C) rs9260155(G;G)
Reference Rs9260155(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911239T; NC_000006.11:g.29911239T>A; NC_000006.11:g.29911239T>C; NC_000006.11:g.29911239T>G
CLNSRC
CLNACC