rs4650135
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4650135(C;C) |
Make rs4650135(C;T) |
Make rs4650135(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 69219314 |
Gene | LOC105378786, LOC105378787 |
is a | snp |
is | mentioned by |
dbSNP | rs4650135 |
dbSNP (classic) | rs4650135 |
ClinGen | rs4650135 |
ebi | rs4650135 |
HLI | rs4650135 |
Exac | rs4650135 |
Gnomad | rs4650135 |
Varsome | rs4650135 |
LitVar | rs4650135 |
Map | rs4650135 |
PheGenI | rs4650135 |
Biobank | rs4650135 |
1000 genomes | rs4650135 |
hgdp | rs4650135 |
ensembl | rs4650135 |
geneview | rs4650135 |
scholar | rs4650135 |
rs4650135 | |
pharmgkb | rs4650135 |
gwascentral | rs4650135 |
openSNP | rs4650135 |
23andMe | rs4650135 |
SNPshot | rs4650135 |
SNPdbe | rs4650135 |
MSV3d | rs4650135 |
GWAS Ctlg | rs4650135 |
GMAF | 0.2571 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18821565] |
Trait | Inattentive symptoms |
Title | Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations |
Risk Allele | |
P-val | 0.000005 |
Odds Ratio | NR NR |