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rs9256983

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9256983(A;T)
Make rs9256983(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943451
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9256983
ebirs9256983
HLIrs9256983
Exacrs9256983
Varsomers9256983
Maprs9256983
PheGenIrs9256983
hapmaprs9256983
1000 genomesrs9256983
hgdprs9256983
ensemblrs9256983
gopubmedrs9256983
geneviewrs9256983
scholarrs9256983
googlers9256983
pharmgkbrs9256983
gwascentralrs9256983
openSNPrs9256983
23andMers9256983
23andMe allrs9256983
SNP Nexus

SNPshotrs9256983
SNPdbers9256983
MSV3drs9256983
GWAS Ctlgrs9256983
GMAF0.2567
Max Magnitude0
ClinVar
Risk rs9256983(C,G,T;C,G,T)
Alt rs9256983(C,G,T;C,G,T)
Reference rs9256983(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911228A; NC_000006.11:g.29911228A>C; NC_000006.11:g.29911228A>G; NC_000006.11:g.29911228A>T
CLNSRC
CLNACC


GET Evidence
HLA-A-E176A
aa_change Glu176Ala
aa_change_short E176A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.257576
summary