IGLON5
IgLON family member 5
Summary
Predicted to act upstream of or within motor behavior and neuromuscular process controlling balance. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1013762278 | 19:51,815,105 | C/G | — | uncertain significance |
| rs765466638 | 19:51,815,106 | C/T | — | uncertain significance |
| rs576949224 | 19:51,815,108 | C/A | — | uncertain significance |
| rs544011313 | 19:51,815,109 | C/A | — | uncertain significance |
| rs754919683 | 19:51,815,111 | C/G | — | uncertain significance |
| rs529762460 | 19:51,815,112 | C/G | — | uncertain significance |
| rs1229876567 | 19:51,815,132 | C/T | — | uncertain significance |
| rs774002619 | 19:51,815,148 | C/T | — | uncertain significance |
| rs180684409 | 19:51,819,239 | C/T | intron variant | — |
| rs149671592 | 19:51,822,506 | C/T | regulatory region variant | — |
| rs143108505 | 19:51,824,517 | C/T | intron variant | — |
| rs752628449 | 19:51,825,327 | C/G | — | uncertain significance |
| rs777145343 | 19:51,825,356 | G/A | — | uncertain significance |
| rs151144652 | 19:51,826,380 | C/G | intron variant | — |
| rs779810845 | 19:51,826,942 | G/A | — | uncertain significance |
| rs779258029 | 19:51,826,980 | G/A | — | uncertain significance |
| rs762038802 | 19:51,827,070 | G/A | — | uncertain significance |
| rs914467184 | 19:51,827,083 | T/C | — | uncertain significance |
| rs2514113969 | 19:51,827,129 | G/C | — | uncertain significance |
| rs369523136 | 19:51,828,624 | C/T | — | uncertain significance |
| rs752899557 | 19:51,828,654 | A/G | — | uncertain significance |
| rs753948923 | 19:51,828,662 | C/G | — | uncertain significance |
| rs761948707 | 19:51,830,077 | G/A | — | uncertain significance |
| rs1343742459 | 19:51,830,149 | A/T | — | uncertain significance |
| rs117206276 | 19:51,830,297 | C/T | regulatory region variant | — |
| rs752432131 | 19:51,830,354 | G/C | — | uncertain significance |
| rs2514117826 | 19:51,830,412 | C/T | — | uncertain significance |
| rs1243685987 | 19:51,830,991 | G/A | — | uncertain significance |
| rs368425289 | 19:51,830,992 | C/G | — | uncertain significance |
| rs539168183 | 19:51,831,024 | C/A | — | uncertain significance |
| rs1568459986 | 19:51,831,087 | C/A | — | uncertain significance |
| rs754365665 | 19:51,831,941 | G/T | — | uncertain significance |
| rs1326195811 | 19:51,831,985 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.