SMTNL2
smoothelin like 2
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1909264055 | 17:4,487,911 | C/T | — | uncertain significance |
| rs993702801 | 17:4,487,919 | G/T | — | uncertain significance |
| rs1024766338 | 17:4,487,923 | A/G | — | uncertain significance |
| rs1306128603 | 17:4,487,925 | G/A | — | uncertain significance |
| rs565052886 | 17:4,487,928 | G/C | — | uncertain significance |
| rs1165308457 | 17:4,487,941 | G/C | — | uncertain significance |
| rs550789809 | 17:4,488,005 | G/C | — | uncertain significance |
| rs538272125 | 17:4,488,144 | G/A | — | uncertain significance |
| rs1909276800 | 17:4,488,160 | C/T | — | uncertain significance |
| rs1260779140 | 17:4,488,192 | G/A | — | uncertain significance |
| rs966658868 | 17:4,488,208 | C/T | — | uncertain significance |
| rs2507927830 | 17:4,488,256 | G/C | — | uncertain significance |
| rs199790658 | 17:4,495,660 | T/C | — | uncertain significance |
| rs960562121 | 17:4,495,710 | T/C | — | uncertain significance |
| rs145126598 | 17:4,496,261 | C/A | — | likely benign |
| rs369073599 | 17:4,496,274 | C/G | — | uncertain significance |
| rs2507938575 | 17:4,496,283 | C/T | — | uncertain significance |
| rs557287522 | 17:4,496,286 | C/T | — | uncertain significance |
| rs556796500 | 17:4,496,308 | G/A | — | uncertain significance |
| rs2507938739 | 17:4,496,322 | C/G | — | uncertain significance |
| rs752233839 | 17:4,496,343 | G/A | — | uncertain significance |
| rs553304059 | 17:4,496,420 | C/G | — | uncertain significance |
| rs376604577 | 17:4,496,443 | C/T | — | uncertain significance |
| rs778604003 | 17:4,497,121 | G/T | — | likely benign |
| rs140742014 | 17:4,497,164 | G/A | — | uncertain significance |
| rs200282407 | 17:4,497,186 | G/A | missense variant | — |
| rs1408815723 | 17:4,498,444 | C/T | — | uncertain significance |
| rs1046651219 | 17:4,498,466 | C/T | — | uncertain significance |
| rs142209104 | 17:4,498,522 | C/T | — | uncertain significance |
| rs200229568 | 17:4,498,523 | G/A | — | uncertain significance |
| rs548022143 | 17:4,498,547 | C/T | — | uncertain significance |
| rs769000793 | 17:4,498,556 | G/A | — | uncertain significance |
| rs374978483 | 17:4,498,576 | C/T | — | uncertain significance |
| rs376330091 | 17:4,498,610 | C/T | — | uncertain significance |
| rs199710091 | 17:4,500,190 | C/T | — | uncertain significance |
| rs1243420034 | 17:4,500,202 | G/C | — | uncertain significance |
| rs367785658 | 17:4,500,240 | G/A | — | uncertain significance |
| rs2507946183 | 17:4,500,489 | C/T | — | uncertain significance |
| rs749054818 | 17:4,500,576 | C/T | — | uncertain significance |
| rs181941136 | 17:4,500,596 | G/A | — | uncertain significance |
| rs200047727 | 17:4,500,617 | G/A | — | uncertain significance |
| rs780405061 | 17:4,510,730 | G/A | — | uncertain significance |
| rs150120447 | 17:4,510,777 | G/A | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.