rs61361928
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common genotype |
Make rs61361928(C;C) |
Make rs61361928(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 4 |
Position | 69096657 |
Gene | UGT2B7 |
is a | snp |
is | mentioned by |
dbSNP | rs61361928 |
dbSNP (classic) | rs61361928 |
ClinGen | rs61361928 |
ebi | rs61361928 |
HLI | rs61361928 |
Exac | rs61361928 |
Gnomad | rs61361928 |
Varsome | rs61361928 |
LitVar | rs61361928 |
Map | rs61361928 |
PheGenI | rs61361928 |
Biobank | rs61361928 |
1000 genomes | rs61361928 |
hgdp | rs61361928 |
ensembl | rs61361928 |
geneview | rs61361928 |
scholar | rs61361928 |
rs61361928 | |
pharmgkb | rs61361928 |
gwascentral | rs61361928 |
openSNP | rs61361928 |
23andMe | rs61361928 |
SNPshot | rs61361928 |
SNPdbe | rs61361928 |
MSV3d | rs61361928 |
GWAS Ctlg | rs61361928 |
Max Magnitude | 0 |
[PMID 25935875] Effect of genetic variations on ticagrelor plasma levels and clinical outcomes