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rs9260157

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs9260157(C;T)
Make rs9260157(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943469
GeneHLA-A
is asnp
is mentioned by
dbSNPrs9260157
ebirs9260157
HLIrs9260157
Exacrs9260157
Varsomers9260157
Maprs9260157
PheGenIrs9260157
hapmaprs9260157
1000 genomesrs9260157
hgdprs9260157
ensemblrs9260157
gopubmedrs9260157
geneviewrs9260157
scholarrs9260157
googlers9260157
pharmgkbrs9260157
gwascentralrs9260157
openSNPrs9260157
23andMers9260157
23andMe allrs9260157
SNP Nexus

SNPshotrs9260157
SNPdbers9260157
MSV3drs9260157
GWAS Ctlgrs9260157
GMAF0.06612
Max Magnitude0
ClinVar
Risk rs9260157(G,T;G,T)
Alt rs9260157(G,T;G,T)
Reference rs9260157(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911246C; NC_000006.11:g.29911246C>G; NC_000006.11:g.29911246C>T
CLNSRC
CLNACC


GET Evidence
HLA-A-A182V
aa_change Ala182Val
aa_change_short A182V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0928896
summary