rs767531
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common genotype |
Make rs767531(A;C) |
Make rs767531(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 35777904 |
is a | snp |
is | mentioned by |
dbSNP | rs767531 |
dbSNP (classic) | rs767531 |
ClinGen | rs767531 |
ebi | rs767531 |
HLI | rs767531 |
Exac | rs767531 |
Gnomad | rs767531 |
Varsome | rs767531 |
LitVar | rs767531 |
Map | rs767531 |
PheGenI | rs767531 |
Biobank | rs767531 |
1000 genomes | rs767531 |
hgdp | rs767531 |
ensembl | rs767531 |
geneview | rs767531 |
scholar | rs767531 |
rs767531 | |
pharmgkb | rs767531 |
gwascentral | rs767531 |
openSNP | rs767531 |
23andMe | rs767531 |
SNPshot | rs767531 |
SNPdbe | rs767531 |
MSV3d | rs767531 |
GWAS Ctlg | rs767531 |
GMAF | 0.0753 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 24223155] Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 18
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d