FNDC1
fibronectin type III domain containing 1
Summary
Predicted to act upstream of or within several processes, including cellular response to hypoxia; positive regulation of cardiac muscle cell apoptotic process; and positive regulation of protein phosphorylation. Predicted to be located in cell-cell junction; mitochondrial membrane; and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants185 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1012166358 | 6:159,590,660 | C/G | — | uncertain significance |
| rs568662089 | 6:159,590,713 | G/T | — | uncertain significance |
| rs534463114 | 6:159,590,729 | C/A | — | uncertain significance |
| rs295332 | 6:159,590,734 | T/A | — | uncertain significance |
| rs578109231 | 6:159,609,113 | A/C | — | — |
| rs616036 | 6:159,614,346 | G/A | intron variant | — |
| rs371692854 | 6:159,618,465 | G/C | — | uncertain significance |
| rs375554497 | 6:159,618,531 | G/A | — | uncertain significance |
| rs890764148 | 6:159,618,547 | C/A | — | uncertain significance |
| rs200625287 | 6:159,618,625 | C/T | — | uncertain significance |
| rs1368881325 | 6:159,618,654 | G/T | — | uncertain significance |
| rs747267222 | 6:159,621,036 | G/T | — | uncertain significance |
| rs1162951650 | 6:159,621,064 | A/G | — | uncertain significance |
| rs201458814 | 6:159,621,084 | C/T | — | uncertain significance |
| rs2482869495 | 6:159,621,108 | C/T | — | uncertain significance |
| rs771300833 | 6:159,621,557 | T/C | — | uncertain significance |
| rs766113964 | 6:159,621,607 | G/A | — | uncertain significance |
| rs774630537 | 6:159,636,009 | C/T | — | uncertain significance |
| rs759316968 | 6:159,636,010 | G/A | — | uncertain significance |
| rs762962324 | 6:159,636,015 | C/T | — | uncertain significance |
| rs764191268 | 6:159,636,016 | G/A | — | uncertain significance |
| rs1782682973 | 6:159,636,087 | T/C | — | uncertain significance |
| rs377525008 | 6:159,636,091 | G/A | — | uncertain significance |
| rs2482892085 | 6:159,636,117 | A/T | — | uncertain significance |
| rs201087585 | 6:159,636,123 | C/T | — | uncertain significance |
| rs2482892121 | 6:159,636,127 | A/G | — | uncertain significance |
| rs148620875 | 6:159,636,167 | C/T | — | benign |
| rs423542 | 6:159,636,316 | A/G | intron variant | — |
| rs371417 | 6:159,639,884 | A/G | intron variant | — |
| rs200289179 | 6:159,642,656 | C/G | — | uncertain significance |
| rs199700478 | 6:159,642,657 | T/G | — | uncertain significance |
| rs756842140 | 6:159,642,717 | G/A | — | uncertain significance |
| rs201387402 | 6:159,644,575 | A/G | — | uncertain significance |
| rs1020433877 | 6:159,644,642 | T/A | — | likely benign |
| rs200234725 | 6:159,644,650 | A/T | — | conflicting classifications of pathogenicity |
| rs365302 | 6:159,646,333 | T/C | intron variant | — |
| rs73595480 | 6:159,646,609 | G/A | — | benign |
| rs2482909679 | 6:159,646,612 | G/T | — | uncertain significance |
| rs370527562 | 6:159,646,688 | C/T | — | uncertain significance |
| rs372105571 | 6:159,647,534 | G/A | — | uncertain significance |
| rs1012901643 | 6:159,647,610 | A/T | — | uncertain significance |
| rs559843888 | 6:159,649,078 | C/T | — | — |
| rs116342739 | 6:159,650,848 | A/G | — | benign |
| rs777699032 | 6:159,650,858 | T/G | — | uncertain significance |
| rs200720425 | 6:159,650,868 | C/T | — | uncertain significance |
| rs376869929 | 6:159,650,895 | C/T | — | uncertain significance |
| rs2482917091 | 6:159,650,904 | A/C | — | uncertain significance |
| rs775787076 | 6:159,650,973 | G/A | — | uncertain significance |
| rs115353623 | 6:159,650,974 | G/A | — | benign |
| rs368131507 | 6:159,651,012 | C/T | — | uncertain significance |
| rs371267836 | 6:159,651,032 | A/G | — | uncertain significance |
| rs201193745 | 6:159,652,910 | G/A | — | benign |
| rs773772923 | 6:159,652,923 | C/A | — | uncertain significance |
| rs750397980 | 6:159,652,961 | G/A | — | uncertain significance |
| rs2482920759 | 6:159,652,982 | C/G | — | uncertain significance |
| rs149582106 | 6:159,653,048 | G/A | — | uncertain significance |
| rs375227070 | 6:159,653,051 | A/G | — | uncertain significance |
| rs891036973 | 6:159,653,154 | C/T | — | uncertain significance |
| rs749539089 | 6:159,653,226 | A/T | — | uncertain significance |
| rs2482921496 | 6:159,653,231 | A/G | — | uncertain significance |
| rs1280017353 | 6:159,653,258 | C/A | — | uncertain significance |
| rs202114028 | 6:159,653,261 | G/A | — | uncertain significance |
| rs762663684 | 6:159,653,307 | T/G | — | uncertain significance |
| rs370836539 | 6:159,653,378 | G/A | — | likely benign |
| rs767784916 | 6:159,653,385 | C/T | — | uncertain significance |
| rs201950696 | 6:159,653,467 | C/A | — | conflicting classifications of pathogenicity |
| rs375412826 | 6:159,653,488 | C/G | — | likely benign |
| rs368778102 | 6:159,653,505 | T/G | — | uncertain significance |
| rs778915395 | 6:159,653,519 | C/T | — | uncertain significance |
| rs754545902 | 6:159,653,564 | C/T | — | uncertain significance |
| rs1317625165 | 6:159,653,591 | G/C | — | uncertain significance |
| rs377692454 | 6:159,653,629 | G/T | — | likely benign |
| rs1783119056 | 6:159,653,630 | C/G | — | uncertain significance |
| rs199926859 | 6:159,653,631 | C/A | — | uncertain significance |
| rs1363667151 | 6:159,653,634 | C/G | — | uncertain significance |
| rs2482923656 | 6:159,653,820 | C/T | — | uncertain significance |
| rs560517397 | 6:159,653,828 | A/G | — | uncertain significance |
| rs2482923756 | 6:159,653,844 | T/A | — | uncertain significance |
| rs146014542 | 6:159,653,891 | G/C | — | uncertain significance |
| rs778461165 | 6:159,653,899 | T/A | — | uncertain significance |
| rs759250812 | 6:159,653,918 | G/C | — | uncertain significance |
| rs2482924609 | 6:159,654,110 | C/G | — | uncertain significance |
| rs200188460 | 6:159,654,128 | C/T | — | uncertain significance |
| rs148688806 | 6:159,654,194 | C/T | — | benign |
| rs760810477 | 6:159,654,227 | C/T | — | likely benign |
| rs779154009 | 6:159,654,348 | A/G | — | likely benign |
| rs369083619 | 6:159,654,458 | A/T | — | uncertain significance |
| rs746040584 | 6:159,654,465 | G/A | — | uncertain significance |
| rs532191873 | 6:159,654,497 | C/G | — | uncertain significance |
| rs750211634 | 6:159,654,500 | T/G | — | uncertain significance |
| rs142239017 | 6:159,654,539 | G/A | — | likely benign |
| rs567210398 | 6:159,654,548 | C/G | — | uncertain significance |
| rs1783158329 | 6:159,654,614 | G/A | — | uncertain significance |
| rs1008907074 | 6:159,654,615 | C/A | — | uncertain significance |
| rs779095363 | 6:159,654,618 | G/A | — | uncertain significance |
| rs1386095241 | 6:159,654,635 | C/T | — | uncertain significance |
| rs773219655 | 6:159,654,684 | G/A | — | uncertain significance |
| rs1187458952 | 6:159,654,686 | C/G | — | uncertain significance |
| rs372992835 | 6:159,654,697 | C/A | — | likely benign |
| rs199539799 | 6:159,654,699 | C/T | — | likely benign |
Showing 100 of 185 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.