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rs179943

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs179943(C;T)
Make rs179943(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position16398087
GeneATXN1
is asnp
is mentioned by
dbSNPrs179943
ebirs179943
HLIrs179943
Exacrs179943
Varsomers179943
Maprs179943
PheGenIrs179943
hapmaprs179943
1000 genomesrs179943
hgdprs179943
ensemblrs179943
gopubmedrs179943
geneviewrs179943
scholarrs179943
googlers179943
pharmgkbrs179943
gwascentralrs179943
openSNPrs179943
23andMers179943
23andMe allrs179943
SNP Nexus

SNPshotrs179943
SNPdbers179943
MSV3drs179943
GWAS Ctlgrs179943
GMAF0.1951
Max Magnitude0
? (C;C) (C;T) (T;T) 28

genomeweb rs4420638 rs11159647 and rs3826656 were also significantly associated with Alzheimer’s disease



[PMID 20308783] Follow-up study of susceptibility Loci for Alzheimer's disease and onset age identified by genome-wide association


GET Evidence
rs179943
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.140625
summary