LRFN5
leucine rich repeat and fibronectin type III domain containing 5
Summary
This gene encodes a protein that belongs to the leucine-rich repeat and fibronectin type III domain-containing family of proteins. A similar protein in mouse, a glycosylated transmembrane protein, is thought to function in presynaptic differentiation. [provided by RefSeq, Sep 2016]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61990288 | 14:42,074,726 | G/A | regulatory region variant | — |
| rs61990289 | 14:42,076,434 | C/T | regulatory region variant | — |
| rs11628299 | 14:42,152,124 | G/A | intron variant | — |
| rs58734839 | 14:42,179,863 | T/C | intron variant | — |
| rs7143983 | 14:42,215,426 | A/T | — | — |
| rs2180231 | 14:42,277,661 | A/G | intron variant | — |
| rs34713514 | 14:42,322,289 | G/A | intron variant | — |
| rs141649332 | 14:42,355,844 | T/C | — | uncertain significance |
| rs755338836 | 14:42,355,972 | C/A | — | uncertain significance |
| rs1886164 | 14:42,356,005 | A/C | — | benign |
| rs151006633 | 14:42,356,086 | A/G | — | likely benign |
| rs139662562 | 14:42,356,180 | A/G | — | uncertain significance |
| rs1215739911 | 14:42,356,244 | C/G | — | uncertain significance |
| rs117966123 | 14:42,356,269 | C/T | — | benign |
| rs905982839 | 14:42,356,295 | A/G | — | uncertain significance |
| rs869312921 | 14:42,356,403 | C/T | — | uncertain significance |
| rs1448844632 | 14:42,356,422 | T/C | — | likely benign |
| rs2139152723 | 14:42,356,616 | G/A | — | uncertain significance |
| rs774680497 | 14:42,356,643 | G/A | — | uncertain significance |
| rs370216412 | 14:42,356,697 | C/T | — | uncertain significance |
| rs150248310 | 14:42,356,773 | G/A | — | likely benign |
| rs746120013 | 14:42,356,822 | A/T | — | uncertain significance |
| rs143251931 | 14:42,356,930 | C/G | — | uncertain significance |
| rs372315722 | 14:42,357,049 | A/G | — | likely benign |
| rs571352632 | 14:42,357,117 | C/T | — | uncertain significance |
| rs1335134922 | 14:42,357,155 | G/A | — | uncertain significance |
| rs2502378550 | 14:42,357,212 | A/G | — | uncertain significance |
| rs574712614 | 14:42,360,542 | A/G | — | uncertain significance |
| rs750924222 | 14:42,360,625 | A/T | — | uncertain significance |
| rs6572117 | 14:42,360,633 | T/C | — | benign |
| rs2502391007 | 14:42,360,697 | T/G | — | likely benign |
| rs2502391176 | 14:42,360,731 | G/T | — | uncertain significance |
| rs150568237 | 14:42,360,758 | C/T | — | uncertain significance |
| rs2502391407 | 14:42,360,767 | G/A | — | uncertain significance |
| rs142220815 | 14:42,360,932 | C/T | — | benign |
| rs746859291 | 14:42,360,937 | A/T | — | uncertain significance |
| rs112647558 | 14:42,361,110 | T/A | — | likely benign |
| rs34676437 | 14:42,361,122 | T/G | — | benign |
| rs1890801648 | 14:42,361,155 | T/G | — | uncertain significance |
| rs116217484 | 14:42,373,369 | G/A | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.