rs766420
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs766420(C;C) |
Make rs766420(C;G) |
Make rs766420(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 154326058 |
Gene | TKTL1 |
is a | snp |
is | mentioned by |
dbSNP | rs766420 |
dbSNP (classic) | rs766420 |
ClinGen | rs766420 |
ebi | rs766420 |
HLI | rs766420 |
Exac | rs766420 |
Gnomad | rs766420 |
Varsome | rs766420 |
LitVar | rs766420 |
Map | rs766420 |
PheGenI | rs766420 |
Biobank | rs766420 |
1000 genomes | rs766420 |
hgdp | rs766420 |
ensembl | rs766420 |
geneview | rs766420 |
scholar | rs766420 |
rs766420 | |
pharmgkb | rs766420 |
gwascentral | rs766420 |
openSNP | rs766420 |
23andMe | rs766420 |
SNPshot | rs766420 |
SNPdbe | rs766420 |
MSV3d | rs766420 |
GWAS Ctlg | rs766420 |
GMAF | 0.3071 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19419973![]() |
Trait | Bilirubin levels |
Title | Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia |
Risk Allele | G |
P-val | 9E-9 |
Odds Ratio | 0.18 [0.12-0.24] SD decrease |