DDAH1
dimethylarginine dimethylaminohydrolase 1
Summary
This gene belongs to the dimethylarginine dimethylaminohydrolase (DDAH) gene family. The encoded enzyme plays a role in nitric oxide generation by regulating cellular concentrations of methylarginines, which in turn inhibit nitric oxide synthase activity. [provided by RefSeq, Jul 2008]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11161597 | 1:85,784,936 | G/A | 3 prime UTR variant | — |
| rs233115 | 1:85,786,977 | G/A | regulatory region variant | — |
| rs1397440289 | 1:85,787,207 | C/T | — | uncertain significance |
| rs752439529 | 1:85,787,227 | T/C | — | uncertain significance |
| rs764088777 | 1:85,790,454 | C/T | — | uncertain significance |
| rs755291583 | 1:85,790,467 | C/T | — | uncertain significance |
| rs1295388167 | 1:85,790,545 | G/A | — | uncertain significance |
| rs28489187 | 1:85,797,110 | A/G | regulatory region variant | — |
| rs233066 | 1:85,804,930 | T/C | regulatory region variant | — |
| rs233069 | 1:85,805,466 | C/T | regulatory region variant | — |
| rs233071 | 1:85,806,005 | C/T | intron variant | — |
| rs2230820 | 1:85,816,134 | T/C | synonymous variant | — |
| rs4949890 | 1:85,830,632 | T/C | intron variant | — |
| rs1431252608 | 1:85,832,798 | G/A | — | — |
| rs2011825 | 1:85,844,671 | T/C | intron variant | — |
| rs997251 | 1:85,845,367 | T/A | — | — |
| rs1884139 | 1:85,845,998 | G/T | intron variant | — |
| rs11161609 | 1:85,862,736 | G/T | intron variant | — |
| rs3949301 | 1:85,863,383 | G/A | intron variant | — |
| rs556982399 | 1:85,876,697 | C/A | — | — |
| rs1554597 | 1:85,877,098 | C/T | intron variant | — |
| rs12138852 | 1:85,878,208 | C/T | intron variant | — |
| rs12123745 | 1:85,884,772 | T/C | intron variant | — |
| rs669173 | 1:85,899,428 | T/C | downstream gene variant | — |
| rs539714 | 1:85,904,338 | C/T | regulatory region variant | — |
| rs57996130 | 1:85,909,013 | T/C | intron variant | — |
| rs12726532 | 1:85,915,373 | T/C | downstream gene variant | — |
| rs11801146 | 1:85,915,374 | C/T | downstream gene variant | — |
| rs877041 | 1:85,923,920 | G/A | intron variant | — |
| rs480414 | 1:85,927,463 | G/A | regulatory region variant | — |
| rs201370663 | 1:85,930,439 | C/T | — | uncertain significance |
| rs2527668775 | 1:85,930,455 | G/C | — | uncertain significance |
| rs2527669385 | 1:85,930,571 | A/G | — | uncertain significance |
| rs769597968 | 1:85,930,610 | A/G | — | uncertain significance |
| rs755171361 | 1:85,930,709 | G/C | — | uncertain significance |
| rs1240759 | 1:85,977,428 | C/G | intron variant | — |
| rs557599360 | 1:85,980,255 | T/C | — | — |
| rs2773130 | 1:85,984,253 | A/G | — | — |
| rs3119165 | 1:85,993,006 | G/C | — | — |
| rs11161637 | 1:86,021,169 | A/T | — | — |
| rs191024636 | 1:86,032,290 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.