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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
ebirs9260155
HLIrs9260155
Exacrs9260155
Varsomers9260155
Maprs9260155
PheGenIrs9260155
hapmaprs9260155
1000 genomesrs9260155
hgdprs9260155
ensemblrs9260155
gopubmedrs9260155
geneviewrs9260155
scholarrs9260155
googlers9260155
pharmgkbrs9260155
gwascentralrs9260155
openSNPrs9260155
23andMers9260155
23andMe allrs9260155
SNP Nexus

SNPshotrs9260155
SNPdbers9260155
MSV3drs9260155
GWAS Ctlgrs9260155
GMAF0.2888
Max Magnitude0
ClinVar
Risk rs9260155(A,C,G;A,C,G)
Alt rs9260155(A,C,G;A,C,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


GET Evidence
HLA-A-L180Q
aa_change Leu180Gln
aa_change_short L180Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.127907
summary