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rs789852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs789852(C;T)
Make rs789852(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position194606369
GeneTMEM44
is asnp
is mentioned by
dbSNPrs789852
ebirs789852
HLIrs789852
Exacrs789852
Varsomers789852
Maprs789852
PheGenIrs789852
hapmaprs789852
1000 genomesrs789852
hgdprs789852
ensemblrs789852
gopubmedrs789852
geneviewrs789852
scholarrs789852
googlers789852
pharmgkbrs789852
gwascentralrs789852
openSNPrs789852
23andMers789852
23andMe allrs789852
SNP Nexus

SNPshotrs789852
SNPdbers789852
MSV3drs789852
GWAS Ctlgrs789852
GMAF0.04867
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20031603OA-icon.png]
Trait QT interval
Title A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations: The EUROSPAN Project
Risk Allele A
P-val 7E-7
Odds Ratio 0.25 [0.15-0.35] unit increase


GET Evidence
rs789852
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.945312
summary