FSD2
fibronectin type III and SPRY domain containing 2
Summary
This gene encodes a protein that belongs to the FN3/SPRY family of proteins. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201393187 | 15:83,428,126 | T/C | — | uncertain significance |
| rs760080782 | 15:83,428,255 | T/C | — | uncertain significance |
| rs2548750776 | 15:83,428,282 | C/T | — | uncertain significance |
| rs774248135 | 15:83,428,294 | G/T | — | uncertain significance |
| rs1039325106 | 15:83,428,339 | A/G | — | uncertain significance |
| rs754677264 | 15:83,428,350 | T/C | — | uncertain significance |
| rs758687087 | 15:83,430,942 | C/G | — | uncertain significance |
| rs2049311237 | 15:83,431,025 | A/C | — | uncertain significance |
| rs117008454 | 15:83,432,161 | T/A | intron variant | — |
| rs757036146 | 15:83,433,975 | C/T | — | uncertain significance |
| rs376563174 | 15:83,433,984 | G/A | — | uncertain significance |
| rs765293776 | 15:83,434,038 | C/T | — | likely benign |
| rs377647056 | 15:83,434,040 | A/C | — | uncertain significance |
| rs201834971 | 15:83,434,652 | A/G | — | likely benign |
| rs1330606951 | 15:83,434,679 | C/T | — | uncertain significance |
| rs759649017 | 15:83,434,683 | C/T | — | uncertain significance |
| rs1354980952 | 15:83,434,688 | G/A | — | uncertain significance |
| rs780944281 | 15:83,434,781 | G/C | — | uncertain significance |
| rs758347169 | 15:83,437,639 | C/T | — | uncertain significance |
| rs780329755 | 15:83,437,668 | G/A | — | uncertain significance |
| rs774888742 | 15:83,437,686 | G/A | — | uncertain significance |
| rs751610449 | 15:83,437,753 | C/T | — | uncertain significance |
| rs766994537 | 15:83,437,771 | G/C | — | uncertain significance |
| rs746987014 | 15:83,438,526 | T/C | — | uncertain significance |
| rs376974776 | 15:83,438,612 | G/A | — | uncertain significance |
| rs181616546 | 15:83,438,799 | G/A | intron variant | — |
| rs374138290 | 15:83,440,831 | G/C | — | uncertain significance |
| rs182674064 | 15:83,440,836 | G/A | — | uncertain significance |
| rs775075067 | 15:83,440,863 | C/T | — | uncertain significance |
| rs751037504 | 15:83,440,897 | C/T | — | uncertain significance |
| rs758413724 | 15:83,440,921 | G/C | — | uncertain significance |
| rs371302622 | 15:83,440,947 | G/A | — | uncertain significance |
| rs536173862 | 15:83,447,608 | C/T | — | uncertain significance |
| rs200246355 | 15:83,447,635 | C/T | — | uncertain significance |
| rs535507046 | 15:83,451,570 | C/T | — | uncertain significance |
| rs1299990598 | 15:83,455,298 | C/T | — | uncertain significance |
| rs1258532574 | 15:83,455,545 | G/C | — | uncertain significance |
| rs374908990 | 15:83,455,641 | C/T | — | uncertain significance |
| rs752459574 | 15:83,455,668 | C/T | — | uncertain significance |
| rs201024587 | 15:83,455,697 | G/A | — | uncertain significance |
| rs376156057 | 15:83,455,740 | C/T | — | uncertain significance |
| rs781225191 | 15:83,455,755 | C/T | — | uncertain significance |
| rs551478249 | 15:83,455,874 | A/G | — | uncertain significance |
| rs767355163 | 15:83,455,883 | C/T | — | uncertain significance |
| rs771361754 | 15:83,455,947 | C/G | — | uncertain significance |
| rs554376766 | 15:83,455,963 | A/T | — | uncertain significance |
| rs760621730 | 15:83,455,988 | G/A | — | uncertain significance |
| rs200540247 | 15:83,465,789 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.