FNDC7
fibronectin type III domain containing 7
Summary
Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs770760027 | 1:109,255,574 | A/T | — | uncertain significance |
| rs1490824528 | 1:109,260,438 | T/C | — | uncertain significance |
| rs986939168 | 1:109,260,474 | C/G | — | uncertain significance |
| rs377221440 | 1:109,260,558 | C/T | — | uncertain significance |
| rs201720195 | 1:109,260,607 | C/A | — | uncertain significance |
| rs545087038 | 1:109,260,608 | G/A | — | uncertain significance |
| rs960051790 | 1:109,261,474 | A/G | — | uncertain significance |
| rs61739598 | 1:109,261,502 | C/T | — | likely benign |
| rs2524376002 | 1:109,264,957 | G/A | — | uncertain significance |
| rs746928344 | 1:109,264,962 | C/T | — | uncertain significance |
| rs942464747 | 1:109,264,975 | A/T | — | uncertain significance |
| rs779911950 | 1:109,265,043 | T/C | — | uncertain significance |
| rs753766216 | 1:109,265,160 | G/A | — | uncertain significance |
| rs4970744 | 1:109,265,642 | C/T | intron variant | — |
| rs57353467 | 1:109,267,367 | C/A | — | — |
| rs2524383007 | 1:109,268,428 | G/C | — | uncertain significance |
| rs1435452557 | 1:109,268,518 | A/C | — | uncertain significance |
| rs2524383525 | 1:109,268,531 | T/A | — | uncertain significance |
| rs2524383566 | 1:109,268,545 | G/A | — | uncertain significance |
| rs1389665574 | 1:109,268,603 | G/T | — | uncertain significance |
| rs747623181 | 1:109,270,493 | G/T | — | uncertain significance |
| rs865904425 | 1:109,270,583 | C/A | — | uncertain significance |
| rs572970288 | 1:109,270,589 | C/T | — | uncertain significance |
| rs377735881 | 1:109,271,310 | G/A | — | uncertain significance |
| rs1411436218 | 1:109,271,320 | G/A | — | likely benign |
| rs140080515 | 1:109,271,361 | G/A | — | uncertain significance |
| rs769004072 | 1:109,271,457 | G/A | — | uncertain significance |
| rs139490781 | 1:109,271,472 | C/T | — | uncertain significance |
| rs766393815 | 1:109,271,473 | G/A | — | uncertain significance |
| rs374062779 | 1:109,271,497 | C/T | — | uncertain significance |
| rs376885498 | 1:109,273,352 | G/A | — | uncertain significance |
| rs377472607 | 1:109,273,409 | A/G | — | uncertain significance |
| rs766519597 | 1:109,273,431 | C/T | — | uncertain significance |
| rs1299705984 | 1:109,273,484 | G/A | — | uncertain significance |
| rs148507979 | 1:109,273,489 | A/G | — | likely benign |
| rs571021394 | 1:109,273,503 | G/A | — | uncertain significance |
| rs2524400874 | 1:109,275,906 | C/T | — | uncertain significance |
| rs748804783 | 1:109,275,947 | C/T | — | uncertain significance |
| rs1348624941 | 1:109,275,972 | G/T | — | uncertain significance |
| rs770019740 | 1:109,276,004 | T/C | — | uncertain significance |
| rs763013847 | 1:109,276,011 | G/C | — | uncertain significance |
| rs200104300 | 1:109,276,020 | C/T | — | uncertain significance |
| rs778504218 | 1:109,276,067 | C/A | — | uncertain significance |
| rs975337251 | 1:109,276,120 | G/T | — | uncertain significance |
| rs749508293 | 1:109,276,137 | C/T | — | uncertain significance |
| rs147592849 | 1:109,280,138 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.