NTN5
netrin 5
Summary
Predicted to be involved in neurogenesis. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants74 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs281391 | 19:49,164,740 | C/T | — | benign |
| rs552076829 | 19:49,164,986 | C/T | — | uncertain significance |
| rs757838150 | 19:49,164,988 | G/A | — | likely benign |
| rs998833186 | 19:49,164,999 | C/T | — | uncertain significance |
| rs770743005 | 19:49,165,022 | C/T | — | uncertain significance |
| rs775613587 | 19:49,165,092 | C/T | — | uncertain significance |
| rs760927020 | 19:49,165,133 | T/C | — | likely benign |
| rs2513926203 | 19:49,165,136 | A/C | — | uncertain significance |
| rs997679907 | 19:49,165,139 | C/T | — | uncertain significance |
| rs549539292 | 19:49,165,157 | A/C | — | likely benign |
| rs1183063421 | 19:49,165,170 | G/A | — | uncertain significance |
| rs750924594 | 19:49,165,196 | C/T | — | uncertain significance |
| rs762414350 | 19:49,165,200 | C/T | — | uncertain significance |
| rs751229571 | 19:49,165,211 | C/A | — | uncertain significance |
| rs927315911 | 19:49,165,224 | C/T | — | uncertain significance |
| rs930033496 | 19:49,165,242 | C/A | — | uncertain significance |
| rs375834403 | 19:49,165,272 | C/T | — | uncertain significance |
| rs150324611 | 19:49,166,741 | T/C | — | likely benign |
| rs562191716 | 19:49,166,744 | G/A | — | uncertain significance |
| rs368089633 | 19:49,166,759 | C/T | — | uncertain significance |
| rs774974345 | 19:49,166,768 | C/T | — | uncertain significance |
| rs1015357976 | 19:49,166,770 | G/A | — | uncertain significance |
| rs371690 | 19:49,166,875 | G/A | — | benign |
| rs1210789356 | 19:49,167,030 | C/T | — | uncertain significance |
| rs149409502 | 19:49,167,065 | G/C | — | uncertain significance |
| rs74418433 | 19:49,167,133 | C/A | — | benign |
| rs73581795 | 19:49,167,361 | A/G | — | benign |
| rs2031625789 | 19:49,167,412 | T/G | — | uncertain significance |
| rs138529881 | 19:49,167,423 | C/A | — | uncertain significance |
| rs777349176 | 19:49,167,451 | G/A | — | uncertain significance |
| rs369282024 | 19:49,167,466 | C/T | — | uncertain significance |
| rs777408698 | 19:49,167,503 | C/G | — | uncertain significance |
| rs1012809089 | 19:49,167,549 | G/A | — | uncertain significance |
| rs184969096 | 19:49,167,778 | C/A | — | benign |
| rs189737503 | 19:49,167,779 | C/T | — | benign |
| rs144755455 | 19:49,167,786 | A/G | — | benign |
| rs114909456 | 19:49,167,851 | G/T | — | uncertain significance |
| rs2031648103 | 19:49,167,926 | G/A | — | uncertain significance |
| rs1166689997 | 19:49,167,935 | G/A | — | uncertain significance |
| rs754816283 | 19:49,167,955 | C/T | — | uncertain significance |
| rs749849106 | 19:49,167,964 | G/A | — | uncertain significance |
| rs2513930258 | 19:49,167,974 | A/G | — | uncertain significance |
| rs201443263 | 19:49,167,993 | G/C | — | uncertain significance |
| rs376771984 | 19:49,167,997 | C/T | — | uncertain significance |
| rs199710487 | 19:49,168,000 | C/T | — | uncertain significance |
| rs17851884 | 19:49,168,005 | A/G | — | benign |
| rs2031653645 | 19:49,168,016 | A/G | — | uncertain significance |
| rs894091364 | 19:49,168,024 | G/A | — | uncertain significance |
| rs373002 | 19:49,168,182 | C/T | — | benign |
| rs448198 | 19:49,168,230 | C/T | — | benign |
| rs925686285 | 19:49,173,633 | C/T | — | likely benign |
| rs752844872 | 19:49,173,649 | G/A | — | uncertain significance |
| rs78031286 | 19:49,173,671 | C/T | — | benign |
| rs902862422 | 19:49,173,672 | G/A | — | uncertain significance |
| rs779342155 | 19:49,173,675 | C/T | — | uncertain significance |
| rs1401508146 | 19:49,173,700 | T/C | — | uncertain significance |
| rs1358841141 | 19:49,173,702 | G/C | — | uncertain significance |
| rs2513938510 | 19:49,173,708 | T/G | — | uncertain significance |
| rs1019910735 | 19:49,173,723 | C/T | — | uncertain significance |
| rs201586895 | 19:49,173,724 | G/A | — | uncertain significance |
| rs767481927 | 19:49,173,730 | G/T | — | uncertain significance |
| rs375822927 | 19:49,173,757 | C/T | — | uncertain significance |
| rs999889884 | 19:49,173,805 | C/T | — | uncertain significance |
| rs766273258 | 19:49,173,819 | A/G | — | uncertain significance |
| rs764251364 | 19:49,173,834 | T/C | — | uncertain significance |
| rs2031932806 | 19:49,173,840 | G/T | — | uncertain significance |
| rs2513938873 | 19:49,173,858 | G/C | — | uncertain significance |
| rs569967296 | 19:49,173,884 | C/A | — | uncertain significance |
| rs2031936774 | 19:49,173,912 | C/G | — | uncertain significance |
| rs373276925 | 19:49,173,945 | C/T | — | uncertain significance |
| rs780849370 | 19:49,174,002 | C/T | — | uncertain significance |
| rs766755719 | 19:49,174,085 | G/T | — | uncertain significance |
| rs553526313 | 19:49,174,129 | C/G | — | uncertain significance |
| rs1176332912 | 19:49,174,160 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.