rs265981
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 |
| Make rs265981(A;G) |
| Make rs265981(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 175443899 |
| Gene | DRD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs265981 |
| dbSNP (classic) | rs265981 |
| ClinGen | rs265981 |
| ebi | rs265981 |
| HLI | rs265981 |
| Exac | rs265981 |
| Gnomad | rs265981 |
| Varsome | rs265981 |
| LitVar | rs265981 |
| Map | rs265981 |
| PheGenI | rs265981 |
| Biobank | rs265981 |
| 1000 genomes | rs265981 |
| hgdp | rs265981 |
| ensembl | rs265981 |
| geneview | rs265981 |
| scholar | rs265981 |
| rs265981 | |
| pharmgkb | rs265981 |
| gwascentral | rs265981 |
| openSNP | rs265981 |
| 23andMe | rs265981 |
| SNPshot | rs265981 |
| SNPdbe | rs265981 |
| MSV3d | rs265981 |
| GWAS Ctlg | rs265981 |
| GMAF | 0.241 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
Implicated as part of a haplotype of the dopamine D1 receptor DRD1 gene associated with autism spectrum disorders in families having only affected males. The haplotype is rs265981(C)-rs4532(A)-rs686(T) as published, though not necessarily as oriented in dbSNP.[PMID 18205172]
[PMID 16380908
] Preferential transmission of paternal alleles at risk genes in attention-deficit/hyperactivity disorder.
[PMID 21955727] An association study between dopamine D1 receptor gene polymorphisms and the risk of schizophrenia.
[PMID 22574669] Dopamine receptors D1 and D2 are related to observed maternal behavior.
