NPR3
natriuretic peptide receptor 3
Summary
This gene encodes one of three natriuretic peptide receptors. Natriutetic peptides are small peptides which regulate blood volume and pressure, pulmonary hypertension, and cardiac function as well as some metabolic and growth processes. The product of this gene encodes a natriuretic peptide receptor responsible for clearing circulating and extracellular natriuretic peptides through endocytosis of the receptor. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011]
Known Variants185 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1458051 | 5:32,689,472 | G/T | — | — |
| rs6450922 | 5:32,689,718 | C/A | — | — |
| rs7729447 | 5:32,689,773 | G/A | intron variant | — |
| rs55665822 | 5:32,705,431 | A/G | intron variant | — |
| rs55738139 | 5:32,705,586 | C/G | — | — |
| rs28513089 | 5:32,710,761 | G/A | — | benign |
| rs572035979 | 5:32,710,786 | G/A | — | benign |
| rs9716700 | 5:32,711,633 | A/C | — | benign |
| rs116204726 | 5:32,711,877 | G/C | — | benign |
| rs562074715 | 5:32,711,890 | C/G | — | uncertain significance |
| rs752039844 | 5:32,711,912 | C/T | — | likely benign |
| rs1170453410 | 5:32,711,915 | G/A | — | likely benign |
| rs1561074170 | 5:32,711,925 | C/G | — | uncertain significance |
| rs979108655 | 5:32,711,933 | G/C | — | uncertain significance |
| rs1252696187 | 5:32,711,936 | G/T | — | likely benign |
| rs1479414238 | 5:32,711,939 | G/C | — | uncertain significance |
| rs1031989391 | 5:32,711,945 | C/G | — | likely benign |
| rs1373301621 | 5:32,711,946 | G/A | — | uncertain significance |
| rs957860113 | 5:32,711,954 | C/T | — | likely benign |
| rs999782749 | 5:32,711,973 | G/A | — | uncertain significance |
| rs1738259169 | 5:32,711,983 | G/A | — | uncertain significance |
| rs1392690210 | 5:32,711,990 | G/A | — | likely benign |
| rs1301392375 | 5:32,712,008 | C/G | — | likely benign |
| rs1738264446 | 5:32,712,028 | C/G | — | uncertain significance |
| rs749467577 | 5:32,712,039 | A/G | — | uncertain significance |
| rs1460036658 | 5:32,712,042 | G/C | — | uncertain significance |
| rs1474213281 | 5:32,712,065 | G/C | — | uncertain significance |
| rs2478213513 | 5:32,712,078 | T/C | — | likely benign |
| rs1325596990 | 5:32,712,100 | G/A | — | uncertain significance |
| rs6859964 | 5:32,712,119 | T/C | — | benign |
| rs1458329208 | 5:32,712,149 | G/C | — | likely benign |
| rs374859010 | 5:32,712,154 | G/T | — | uncertain significance |
| rs756559284 | 5:32,712,156 | C/T | — | uncertain significance |
| rs745984932 | 5:32,712,167 | G/A | — | likely benign |
| rs772129919 | 5:32,712,169 | G/A | — | uncertain significance |
| rs2111840861 | 5:32,712,174 | C/G | — | uncertain significance |
| rs1561074830 | 5:32,712,191 | C/T | — | likely benign |
| rs374236891 | 5:32,712,212 | C/T | — | likely benign |
| rs769527811 | 5:32,712,236 | C/A | — | uncertain significance |
| rs1263411940 | 5:32,712,248 | G/A | — | likely benign |
| rs1020773035 | 5:32,712,264 | C/G | — | uncertain significance |
| rs1202238772 | 5:32,712,269 | C/T | — | likely benign |
| rs754276633 | 5:32,712,299 | A/G | — | likely benign |
| rs1433125500 | 5:32,712,324 | T/C | — | likely pathogenic |
| rs2478215379 | 5:32,712,329 | C/T | — | likely benign |
| rs758483759 | 5:32,712,350 | G/A | — | likely benign |
| rs1228982969 | 5:32,712,398 | G/T | — | likely benign |
| rs776997035 | 5:32,712,415 | C/A | — | uncertain significance |
| rs2111842185 | 5:32,712,432 | A/T | — | uncertain significance |
| rs781249323 | 5:32,712,465 | C/T | — | uncertain significance |
| rs536801135 | 5:32,712,485 | A/G | — | likely benign |
| rs891871524 | 5:32,712,508 | T/A | — | uncertain significance |
| rs377062036 | 5:32,712,539 | G/A | — | likely benign |
| rs770169526 | 5:32,712,565 | G/A | — | uncertain significance |
| rs202144521 | 5:32,712,570 | C/T | — | uncertain significance |
| rs1279843711 | 5:32,712,574 | C/A | — | uncertain significance |
| rs763277450 | 5:32,712,575 | G/A | — | likely benign |
| rs767430720 | 5:32,712,594 | G/C | — | uncertain significance |
| rs2478217648 | 5:32,712,625 | T/C | — | uncertain significance |
| rs2111843383 | 5:32,712,642 | A/G | — | uncertain significance |
| rs746508357 | 5:32,712,645 | G/C | — | uncertain significance |
| rs2111843419 | 5:32,712,647 | G/A | — | likely benign |
| rs377559221 | 5:32,712,659 | G/C | — | likely benign |
| rs371043582 | 5:32,712,668 | C/A | — | likely benign |
| rs771228213 | 5:32,712,669 | C/G | — | likely benign |
| rs1334706432 | 5:32,712,671 | G/C | — | likely benign |
| rs77559951 | 5:32,712,674 | C/T | — | benign |
| rs4867473 | 5:32,712,831 | C/T | — | benign |
| rs3792765 | 5:32,713,836 | A/G | regulatory region variant | — |
| rs1421811 | 5:32,714,270 | C/T | — | — |
| rs2194178 | 5:32,718,044 | C/T | intron variant | — |
| rs6889608 | 5:32,719,693 | C/T | intron variant | — |
| rs113811158 | 5:32,721,116 | G/A | — | — |
| rs374865702 | 5:32,724,794 | C/T | — | likely benign |
| rs1269598391 | 5:32,724,800 | C/T | — | likely benign |
| rs766009777 | 5:32,724,804 | T/C | — | uncertain significance |
| rs186814909 | 5:32,724,806 | G/T | — | conflicting classifications of pathogenicity |
| rs969206323 | 5:32,724,823 | C/T | — | likely benign |
| rs775585104 | 5:32,724,837 | G/A | — | uncertain significance |
| rs933468549 | 5:32,724,854 | G/A | — | uncertain significance |
| rs374966067 | 5:32,724,855 | C/T | — | uncertain significance |
| rs139065863 | 5:32,724,856 | G/A | — | benign |
| rs374205048 | 5:32,724,886 | C/T | — | likely benign |
| rs767132770 | 5:32,724,887 | G/A | — | uncertain significance |
| rs1316577485 | 5:32,724,922 | C/A | — | likely benign |
| rs200820724 | 5:32,724,942 | C/A | — | benign |
| rs1147224 | 5:32,725,072 | T/C | — | benign |
| rs700923 | 5:32,734,868 | A/T | — | — |
| rs55871801 | 5:32,738,758 | A/G | — | benign |
| rs2292025 | 5:32,738,886 | G/A | — | benign |
| rs2292026 | 5:32,738,891 | C/T | — | benign |
| rs372211082 | 5:32,738,960 | T/C | — | likely benign |
| rs767222632 | 5:32,738,993 | G/A | — | uncertain significance |
| rs750920406 | 5:32,739,011 | G/A | — | uncertain significance |
| rs765541392 | 5:32,739,028 | G/A | — | likely benign |
| rs151246481 | 5:32,739,121 | C/T | — | likely benign |
| rs752059527 | 5:32,739,137 | G/A | — | conflicting classifications of pathogenicity |
| rs201661872 | 5:32,739,143 | G/A | — | likely benign |
| rs817898 | 5:32,739,289 | G/T | — | benign |
| rs79938890 | 5:32,739,291 | T/G | — | benign |
Showing 100 of 185 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.