SAMD3
sterile alpha motif domain containing 3
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs773652776 | 6:130,465,687 | C/T | — | uncertain significance |
| rs367601593 | 6:130,465,691 | C/T | — | uncertain significance |
| rs767707486 | 6:130,465,811 | A/G | — | uncertain significance |
| rs368648301 | 6:130,465,822 | A/G | — | uncertain significance |
| rs201831635 | 6:130,465,847 | C/T | — | likely benign |
| rs140284624 | 6:130,465,850 | C/T | — | uncertain significance |
| rs369863649 | 6:130,465,916 | T/G | — | uncertain significance |
| rs1788527354 | 6:130,466,525 | A/G | — | uncertain significance |
| rs1788595861 | 6:130,467,180 | A/T | — | likely benign |
| rs1192244520 | 6:130,467,181 | T/A | — | uncertain significance |
| rs41285306 | 6:130,467,238 | G/A | missense variant | — |
| rs2536020241 | 6:130,467,250 | T/C | — | uncertain significance |
| rs1000039284 | 6:130,467,260 | A/G | — | uncertain significance |
| rs749467124 | 6:130,467,278 | T/G | — | uncertain significance |
| rs775960481 | 6:130,475,989 | A/G | — | uncertain significance |
| rs200849847 | 6:130,497,047 | C/T | — | uncertain significance |
| rs144450186 | 6:130,505,271 | G/C | — | uncertain significance |
| rs746454475 | 6:130,505,304 | C/T | — | uncertain significance |
| rs956208350 | 6:130,505,610 | T/C | — | uncertain significance |
| rs758222319 | 6:130,505,679 | C/G | — | uncertain significance |
| rs930859093 | 6:130,505,760 | A/G | — | uncertain significance |
| rs34209761 | 6:130,516,412 | C/T | intron variant | — |
| rs112197738 | 6:130,530,653 | C/A | — | uncertain significance |
| rs371148224 | 6:130,530,713 | C/T | — | uncertain significance |
| rs138130162 | 6:130,530,720 | C/A | — | likely benign |
| rs1010788005 | 6:130,530,748 | C/G | — | uncertain significance |
| rs143283725 | 6:130,535,545 | C/T | — | likely benign |
| rs139187903 | 6:130,535,551 | G/A | — | uncertain significance |
| rs143580700 | 6:130,535,602 | A/G | — | uncertain significance |
| rs193004422 | 6:130,535,651 | C/T | — | uncertain significance |
| rs10447419 | 6:130,550,063 | C/T | — | — |
| rs181078317 | 6:130,560,650 | T/A | intron variant | — |
| rs4897393 | 6:130,597,270 | A/G | intron variant | — |
| rs75467494 | 6:130,630,235 | G/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.