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rs9260156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9260156(G;G)
Make rs9260156(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943463
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260156
ebirs9260156
HLIrs9260156
Exacrs9260156
Varsomers9260156
Maprs9260156
PheGenIrs9260156
hapmaprs9260156
1000 genomesrs9260156
hgdprs9260156
ensemblrs9260156
gopubmedrs9260156
geneviewrs9260156
scholarrs9260156
googlers9260156
pharmgkbrs9260156
gwascentralrs9260156
openSNPrs9260156
23andMers9260156
23andMe allrs9260156
SNP Nexus

SNPshotrs9260156
SNPdbers9260156
MSV3drs9260156
GWAS Ctlgrs9260156
GMAF0.2773
Max Magnitude0
ClinVar
Risk rs9260156(A,G;A,G)
Alt rs9260156(A,G;A,G)
Reference rs9260156(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911240T; NC_000006.11:g.29911240T>A; NC_000006.11:g.29911240T>G
CLNSRC
CLNACC


GET Evidence
HLA-A-L180W
aa_change Leu180Trp
aa_change_short L180W
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.266586
summary