NIPAL3
NIPA like domain containing 3
Summary
Predicted to enable magnesium ion transmembrane transporter activity. Predicted to be involved in magnesium ion transport. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs554348123 | 1:24,741,313 | G/C | — | — |
| rs139905565 | 1:24,742,324 | C/T | — | benign |
| rs749273872 | 1:24,746,055 | C/A | — | uncertain significance |
| rs148391167 | 1:24,746,056 | G/A | — | benign |
| rs2294521 | 1:24,746,127 | C/T | — | benign |
| rs192637449 | 1:24,766,183 | G/A | intron variant | — |
| rs766406791 | 1:24,766,663 | A/C | — | uncertain significance |
| rs149829624 | 1:24,768,560 | C/T | — | uncertain significance |
| rs768764094 | 1:24,768,587 | G/A | — | uncertain significance |
| rs199698296 | 1:24,768,603 | A/G | — | uncertain significance |
| rs1434551086 | 1:24,768,650 | G/A | — | uncertain significance |
| rs147193388 | 1:24,768,665 | G/A | — | uncertain significance |
| rs776685672 | 1:24,768,711 | T/A | — | uncertain significance |
| rs775690499 | 1:24,771,720 | C/T | — | uncertain significance |
| rs144375095 | 1:24,771,721 | G/A | — | likely benign |
| rs1200038240 | 1:24,776,066 | G/A | — | uncertain significance |
| rs780800864 | 1:24,776,099 | C/T | — | uncertain significance |
| rs369779259 | 1:24,779,910 | A/G | — | likely benign |
| rs778923639 | 1:24,779,920 | G/A | — | uncertain significance |
| rs773822376 | 1:24,779,986 | C/T | — | uncertain significance |
| rs112615347 | 1:24,782,656 | C/T | — | likely benign |
| rs151040412 | 1:24,782,681 | A/G | — | uncertain significance |
| rs761484348 | 1:24,782,692 | C/G | — | uncertain significance |
| rs765130708 | 1:24,782,699 | C/T | — | uncertain significance |
| rs778162926 | 1:24,782,732 | T/C | — | uncertain significance |
| rs185614655 | 1:24,785,406 | G/C | — | uncertain significance |
| rs1049690872 | 1:24,786,979 | T/G | — | uncertain significance |
| rs542124168 | 1:24,786,997 | G/A | — | uncertain significance |
| rs764114672 | 1:24,787,021 | A/T | — | uncertain significance |
| rs195720 | 1:24,787,947 | A/T | — | — |
| rs195722 | 1:24,788,128 | A/T | — | — |
| rs150020630 | 1:24,795,472 | T/A | — | benign |
| rs202117908 | 1:24,795,495 | T/C | — | likely benign |
| rs758119841 | 1:24,795,508 | G/A | — | uncertain significance |
| rs2521367220 | 1:24,795,512 | A/G | — | uncertain significance |
| rs762832290 | 1:24,795,589 | A/G | — | uncertain significance |
| rs147661477 | 1:24,795,618 | C/T | — | likely benign |
| rs750515682 | 1:24,795,640 | C/G | — | uncertain significance |
| rs780304529 | 1:24,795,644 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.