IGSF3
immunoglobulin superfamily member 3
Summary
The protein encoded by this gene is an immunoglobulin-like membrane protein containing several V-type Ig-like domains. A mutation in this gene has been associated with bilateral nasolacrimal duct obstruction (LCDD). [provided by RefSeq, Jun 2016]
Known Variants112 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs116610628 | 1:117,119,741 | T/C | — | — |
| rs1180134483 | 1:117,119,950 | G/C | — | uncertain significance |
| rs531326462 | 1:117,120,065 | G/A | — | uncertain significance |
| rs1189914440 | 1:117,120,088 | A/T | — | uncertain significance |
| rs2525127768 | 1:117,120,092 | T/C | — | uncertain significance |
| rs368581214 | 1:117,120,149 | C/T | — | uncertain significance |
| rs1171428752 | 1:117,120,154 | T/C | — | uncertain significance |
| rs372235081 | 1:117,122,028 | C/T | — | likely benign |
| rs976266015 | 1:117,122,029 | G/A | — | uncertain significance |
| rs755995207 | 1:117,122,043 | G/A | — | uncertain significance |
| rs761076449 | 1:117,122,048 | C/G | — | uncertain significance |
| rs200409720 | 1:117,122,105 | A/G | — | likely benign |
| rs6703791 | 1:117,122,130 | T/C | — | benign |
| rs767375748 | 1:117,122,272 | C/T | — | uncertain significance |
| rs540876761 | 1:117,122,284 | C/T | — | uncertain significance |
| rs114915440 | 1:117,122,285 | G/C | — | benign |
| rs647711 | 1:117,122,288 | G/C | — | benign |
| rs1233679735 | 1:117,122,303 | C/G | — | uncertain significance |
| rs549588340 | 1:117,122,332 | G/C | — | uncertain significance |
| rs141418874 | 1:117,122,355 | C/G | — | uncertain significance |
| rs2525145113 | 1:117,122,367 | C/T | — | uncertain significance |
| rs764947089 | 1:117,122,389 | C/A | — | uncertain significance |
| rs138319827 | 1:117,122,466 | T/C | — | uncertain significance |
| rs549817217 | 1:117,126,199 | T/C | — | — |
| rs201362284 | 1:117,127,301 | G/C | — | likely benign |
| rs2525173364 | 1:117,127,383 | T/G | — | uncertain significance |
| rs749216309 | 1:117,127,411 | G/T | — | uncertain significance |
| rs41301291 | 1:117,127,417 | T/C | — | benign |
| rs370299026 | 1:117,127,420 | C/T | — | uncertain significance |
| rs149962221 | 1:117,127,421 | G/A | — | likely benign |
| rs41299557 | 1:117,127,495 | C/T | — | uncertain significance |
| rs142344210 | 1:117,127,509 | C/T | — | uncertain significance |
| rs1196990837 | 1:117,127,525 | G/A | — | uncertain significance |
| rs777455675 | 1:117,127,533 | T/A | — | uncertain significance |
| rs899569190 | 1:117,127,541 | C/T | — | likely benign |
| rs2525175300 | 1:117,127,549 | C/T | — | uncertain significance |
| rs1571118438 | 1:117,127,565 | G/T | — | likely benign |
| rs76503986 | 1:117,127,644 | C/T | — | benign |
| rs199709861 | 1:117,127,655 | G/C | — | uncertain significance |
| rs17036023 | 1:117,129,711 | A/G | regulatory region variant | — |
| rs1441070038 | 1:117,131,342 | C/T | — | uncertain significance |
| rs769995025 | 1:117,131,408 | T/A | — | uncertain significance |
| rs761730940 | 1:117,131,439 | C/T | — | uncertain significance |
| rs2525199086 | 1:117,131,577 | C/T | — | uncertain significance |
| rs2525199155 | 1:117,131,583 | C/T | — | uncertain significance |
| rs2525199907 | 1:117,131,681 | A/G | — | uncertain significance |
| rs2525200021 | 1:117,131,695 | C/G | — | uncertain significance |
| rs775946454 | 1:117,142,640 | C/T | — | uncertain significance |
| rs371958247 | 1:117,142,691 | C/T | — | uncertain significance |
| rs190300523 | 1:117,142,751 | C/A | — | uncertain significance |
| rs372102204 | 1:117,142,788 | C/T | — | uncertain significance |
| rs144247428 | 1:117,142,793 | C/T | — | uncertain significance |
| rs751185422 | 1:117,142,794 | G/A | — | uncertain significance |
| rs1302805214 | 1:117,142,827 | T/G | — | uncertain significance |
| rs199596005 | 1:117,142,835 | G/A | — | likely benign |
| rs200735353 | 1:117,142,845 | G/A | — | uncertain significance |
| rs61730489 | 1:117,142,868 | C/T | — | pathogenic |
| rs748633506 | 1:117,142,910 | G/T | — | uncertain significance |
| rs372163033 | 1:117,142,914 | C/T | — | uncertain significance |
| rs138769450 | 1:117,142,956 | C/T | — | uncertain significance |
| rs376119768 | 1:117,142,964 | A/G | — | likely benign |
| rs1660683262 | 1:117,146,252 | C/T | — | uncertain significance |
| rs61730488 | 1:117,146,376 | G/A | — | likely benign |
| rs2525274198 | 1:117,146,393 | A/C | — | uncertain significance |
| rs370022674 | 1:117,146,420 | C/T | — | likely benign |
| rs150918555 | 1:117,146,542 | C/T | — | uncertain significance |
| rs1660697272 | 1:117,146,561 | C/T | — | uncertain significance |
| rs752933561 | 1:117,146,584 | C/T | — | likely benign |
| rs1249882495 | 1:117,146,643 | G/C | — | uncertain significance |
| rs41275572 | 1:117,146,698 | G/A | intron variant | — |
| rs759366082 | 1:117,150,627 | C/T | — | uncertain significance |
| rs202203327 | 1:117,150,686 | C/A | — | uncertain significance |
| rs138298816 | 1:117,150,687 | G/A | — | uncertain significance |
| rs2525295038 | 1:117,150,689 | A/T | — | uncertain significance |
| rs201314078 | 1:117,150,693 | G/A | — | uncertain significance |
| rs375451086 | 1:117,150,699 | T/A | — | uncertain significance |
| rs751811650 | 1:117,150,855 | C/T | — | uncertain significance |
| rs191438836 | 1:117,150,856 | G/A | — | benign |
| rs373355041 | 1:117,150,896 | G/A | — | uncertain significance |
| rs765984344 | 1:117,150,908 | G/A | — | uncertain significance |
| rs78612004 | 1:117,150,918 | G/T | — | benign |
| rs199569798 | 1:117,150,939 | C/T | — | uncertain significance |
| rs376055846 | 1:117,156,422 | C/T | — | uncertain significance |
| rs376632014 | 1:117,156,471 | C/T | — | uncertain significance |
| rs765347295 | 1:117,156,474 | C/T | — | uncertain significance |
| rs1321287848 | 1:117,156,492 | C/T | — | uncertain significance |
| rs772523287 | 1:117,156,508 | C/G | — | uncertain significance |
| rs1425031432 | 1:117,156,528 | G/A | — | uncertain significance |
| rs143287450 | 1:117,156,531 | G/A | missense variant | — |
| rs1459776835 | 1:117,156,551 | T/C | — | uncertain significance |
| rs530464588 | 1:117,156,665 | C/A | — | uncertain significance |
| rs1448888822 | 1:117,156,702 | T/A | — | uncertain significance |
| rs749460351 | 1:117,156,734 | G/A | — | uncertain significance |
| rs532322659 | 1:117,156,753 | G/A | — | uncertain significance |
| rs1288839496 | 1:117,156,755 | A/G | — | uncertain significance |
| rs367708710 | 1:117,158,778 | G/A | — | likely benign |
| rs775220134 | 1:117,158,823 | C/T | — | likely benign |
| rs1197430180 | 1:117,158,839 | A/G | — | uncertain significance |
| rs544303323 | 1:117,158,855 | C/T | — | uncertain significance |
| rs754395956 | 1:117,158,858 | G/A | — | uncertain significance |
Showing 100 of 112 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.