rs16973500
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16973500(C;C) |
Make rs16973500(C;T) |
Make rs16973500(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 71931293 |
Gene | PKD1L3 |
is a | snp |
is | mentioned by |
dbSNP | rs16973500 |
dbSNP (classic) | rs16973500 |
ClinGen | rs16973500 |
ebi | rs16973500 |
HLI | rs16973500 |
Exac | rs16973500 |
Gnomad | rs16973500 |
Varsome | rs16973500 |
LitVar | rs16973500 |
Map | rs16973500 |
PheGenI | rs16973500 |
Biobank | rs16973500 |
1000 genomes | rs16973500 |
hgdp | rs16973500 |
ensembl | rs16973500 |
geneview | rs16973500 |
scholar | rs16973500 |
rs16973500 | |
pharmgkb | rs16973500 |
gwascentral | rs16973500 |
openSNP | rs16973500 |
23andMe | rs16973500 |
SNPshot | rs16973500 |
SNPdbe | rs16973500 |
MSV3d | rs16973500 |
GWAS Ctlg | rs16973500 |
GMAF | 0.1763 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18951430] |
Trait | Attention-deficit/hyperactivity disorder and conduct disorder |
Title | Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study |
Risk Allele | C |
P-val | 0.000007 |
Odds Ratio | NR NR |