Have questions? Visit https://www.reddit.com/r/SNPedia

rs767531

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common genotype
Make rs767531(A;C)
Make rs767531(C;C)
ReferenceGRCh38 38.1/141
Chromosome18
Position35777904
is asnp
is mentioned by
dbSNPrs767531
dbSNP (classic)rs767531
ClinGenrs767531
ebirs767531
HLIrs767531
Exacrs767531
Gnomadrs767531
Varsomers767531
LitVarrs767531
Maprs767531
PheGenIrs767531
Biobankrs767531
1000 genomesrs767531
hgdprs767531
ensemblrs767531
geneviewrs767531
scholarrs767531
googlers767531
pharmgkbrs767531
gwascentralrs767531
openSNPrs767531
23andMers767531
SNPshotrs767531
SNPdbers767531
MSV3drs767531
GWAS Ctlgrs767531
GMAF0.0753
Max Magnitude0
? (A;A) (A;C) (C;C) 28


[PMID 24223155OA-icon.png] Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes