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rs9256982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9256982(C;C)
Make rs9256982(C;G)
Make rs9256982(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943223
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9256982
ebirs9256982
HLIrs9256982
Exacrs9256982
Varsomers9256982
Maprs9256982
PheGenIrs9256982
hapmaprs9256982
1000 genomesrs9256982
hgdprs9256982
ensemblrs9256982
gopubmedrs9256982
geneviewrs9256982
scholarrs9256982
googlers9256982
pharmgkbrs9256982
gwascentralrs9256982
openSNPrs9256982
23andMers9256982
23andMe allrs9256982
SNP Nexus

SNPshotrs9256982
SNPdbers9256982
MSV3drs9256982
GWAS Ctlgrs9256982
GMAF0.3503
Max Magnitude0
ClinVar
Risk rs9256982(C,G;C,G)
Alt rs9256982(C,G;C,G)
Reference rs9256982(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911000T; NC_000006.11:g.29911000T>C; NC_000006.11:g.29911000T>G
CLNSRC
CLNACC