rs2602381
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2602381(C;C) |
Make rs2602381(C;T) |
Make rs2602381(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 233675678 |
Gene | UGT1A8, UGT1A9, UGT1A10 |
is a | snp |
is | mentioned by |
dbSNP | rs2602381 |
dbSNP (classic) | rs2602381 |
ClinGen | rs2602381 |
ebi | rs2602381 |
HLI | rs2602381 |
Exac | rs2602381 |
Gnomad | rs2602381 |
Varsome | rs2602381 |
LitVar | rs2602381 |
Map | rs2602381 |
PheGenI | rs2602381 |
Biobank | rs2602381 |
1000 genomes | rs2602381 |
hgdp | rs2602381 |
ensembl | rs2602381 |
geneview | rs2602381 |
scholar | rs2602381 |
rs2602381 | |
pharmgkb | rs2602381 |
gwascentral | rs2602381 |
openSNP | rs2602381 |
23andMe | rs2602381 |
SNPshot | rs2602381 |
SNPdbe | rs2602381 |
MSV3d | rs2602381 |
GWAS Ctlg | rs2602381 |
GMAF | 0.4054 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20732626] |
Trait | |
Title | Family-Based Genome-Wide Association Scan of Attention-Deficit/Hyperactivity Disorder |
Risk Allele | A |
P-val | 0.000004 |
Odds Ratio | 1.42 [NR] |