rs2276314
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2276314(A;A) |
Make rs2276314(A;G) |
Make rs2276314(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 35977503 |
Gene | C18orf21 |
is a | snp |
is | mentioned by |
dbSNP | rs2276314 |
dbSNP (classic) | rs2276314 |
ClinGen | rs2276314 |
ebi | rs2276314 |
HLI | rs2276314 |
Exac | rs2276314 |
Gnomad | rs2276314 |
Varsome | rs2276314 |
LitVar | rs2276314 |
Map | rs2276314 |
PheGenI | rs2276314 |
Biobank | rs2276314 |
1000 genomes | rs2276314 |
hgdp | rs2276314 |
ensembl | rs2276314 |
geneview | rs2276314 |
scholar | rs2276314 |
rs2276314 | |
pharmgkb | rs2276314 |
gwascentral | rs2276314 |
openSNP | rs2276314 |
23andMe | rs2276314 |
SNPshot | rs2276314 |
SNPdbe | rs2276314 |
MSV3d | rs2276314 |
GWAS Ctlg | rs2276314 |
GMAF | 0.242 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24223155] Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes