NAV2
neuron navigator 2
Summary
This gene encodes a member of the neuron navigator gene family, which may play a role in cellular growth and migration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]
Known Variants240 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1354269 | 11:19,374,244 | T/C | intron variant | — |
| rs12364788 | 11:19,427,092 | T/G | upstream gene variant | — |
| rs10766557 | 11:19,447,547 | G/T | — | — |
| rs116608994 | 11:19,550,200 | C/T | intron variant | — |
| rs874426 | 11:19,569,563 | C/A | intron variant | — |
| rs10500856 | 11:19,584,502 | A/G | intron variant | — |
| rs11025185 | 11:19,593,806 | G/A | upstream gene variant | — |
| rs10741780 | 11:19,599,971 | T/A | — | — |
| rs143445068 | 11:19,632,396 | G/C | intron variant | — |
| rs140093730 | 11:19,729,684 | T/C | downstream gene variant | — |
| rs1288286466 | 11:19,735,267 | A/C | — | uncertain significance |
| rs764558532 | 11:19,735,272 | A/G | — | uncertain significance |
| rs146393896 | 11:19,735,280 | A/C | — | likely benign |
| rs184978478 | 11:19,735,292 | C/G | — | benign |
| rs755849383 | 11:19,735,293 | G/A | — | uncertain significance |
| rs11828836 | 11:19,735,325 | C/A | — | benign |
| rs951588262 | 11:19,735,348 | C/A | — | uncertain significance |
| rs1219313804 | 11:19,735,369 | G/A | — | uncertain significance |
| rs756079268 | 11:19,735,392 | A/T | — | uncertain significance |
| rs148165391 | 11:19,735,396 | A/G | — | likely benign |
| rs141966195 | 11:19,735,411 | C/G | — | benign |
| rs2050046780 | 11:19,735,438 | T/A | — | uncertain significance |
| rs79661416 | 11:19,823,053 | G/T | intron variant | — |
| rs6483617 | 11:19,854,088 | A/G | — | benign |
| rs148087344 | 11:19,854,095 | C/T | — | likely benign |
| rs2060584824 | 11:19,864,427 | G/T | — | uncertain significance |
| rs1838055 | 11:19,871,230 | G/C | regulatory region variant | — |
| rs761009001 | 11:19,890,504 | G/T | — | uncertain significance |
| rs139902326 | 11:19,890,529 | G/A | — | uncertain significance |
| rs1371745241 | 11:19,901,522 | C/T | — | uncertain significance |
| rs775361258 | 11:19,901,528 | G/A | — | uncertain significance |
| rs750093474 | 11:19,901,546 | G/A | — | uncertain significance |
| rs148928708 | 11:19,901,549 | G/A | — | uncertain significance |
| rs2549685613 | 11:19,901,550 | C/G | — | uncertain significance |
| rs2063101824 | 11:19,901,574 | C/T | — | uncertain significance |
| rs748445088 | 11:19,901,577 | C/T | — | uncertain significance |
| rs770201436 | 11:19,901,588 | G/T | — | uncertain significance |
| rs762725317 | 11:19,901,643 | A/C | — | uncertain significance |
| rs747098080 | 11:19,913,996 | G/A | — | uncertain significance |
| rs200234458 | 11:19,914,033 | G/A | — | uncertain significance |
| rs142341675 | 11:19,914,072 | G/A | missense variant | — |
| rs145926987 | 11:19,914,117 | C/A | — | uncertain significance |
| rs138529273 | 11:19,914,123 | C/T | — | uncertain significance |
| rs76088545 | 11:19,914,133 | C/T | — | benign |
| rs57575249 | 11:19,914,159 | G/A | — | benign |
| rs768271752 | 11:19,954,723 | G/C | — | uncertain significance |
| rs763390531 | 11:19,954,752 | C/T | — | uncertain significance |
| rs150902509 | 11:19,954,775 | G/C | — | uncertain significance |
| rs1414451311 | 11:19,954,778 | T/C | — | uncertain significance |
| rs758235111 | 11:19,954,786 | G/T | — | uncertain significance |
| rs374063856 | 11:19,954,790 | G/A | — | likely benign |
| rs775808548 | 11:19,954,827 | C/T | — | uncertain significance |
| rs367880415 | 11:19,954,836 | C/G | — | uncertain significance |
| rs1052938418 | 11:19,954,908 | T/C | — | uncertain significance |
| rs775021883 | 11:19,955,057 | C/T | — | likely benign |
| rs761755037 | 11:19,955,058 | G/A | — | uncertain significance |
| rs950954384 | 11:19,955,064 | C/T | — | uncertain significance |
| rs148875394 | 11:19,955,110 | G/A | — | likely benign |
| rs1442715154 | 11:19,955,117 | G/T | — | uncertain significance |
| rs1398591681 | 11:19,955,142 | C/T | — | uncertain significance |
| rs374810981 | 11:19,955,144 | G/A | — | uncertain significance |
| rs16937251 | 11:19,955,194 | G/C | — | benign |
| rs2550411096 | 11:19,955,201 | T/C | — | uncertain significance |
| rs548877132 | 11:19,955,244 | A/G | — | conflicting classifications of pathogenicity |
| rs754191884 | 11:19,955,270 | C/T | — | uncertain significance |
| rs147604281 | 11:19,955,322 | C/T | — | benign |
| rs538392113 | 11:19,955,381 | G/A | — | uncertain significance |
| rs765537926 | 11:19,955,383 | G/C | — | uncertain significance |
| rs766754248 | 11:19,955,394 | A/C | — | uncertain significance |
| rs142436930 | 11:19,955,407 | T/C | — | benign |
| rs757038885 | 11:19,955,424 | A/G | — | uncertain significance |
| rs138003585 | 11:19,955,433 | A/T | — | uncertain significance |
| rs149486594 | 11:19,955,465 | C/G | — | uncertain significance |
| rs144761679 | 11:19,955,490 | C/T | — | uncertain significance |
| rs1372989 | 11:19,955,500 | A/G | — | benign |
| rs1264033576 | 11:19,955,502 | G/T | — | uncertain significance |
| rs190496095 | 11:19,955,505 | T/G | — | uncertain significance |
| rs142297156 | 11:19,955,552 | C/T | — | likely benign |
| rs546309991 | 11:19,955,553 | G/A | — | uncertain significance |
| rs139283675 | 11:19,955,559 | G/A | — | uncertain significance |
| rs1270591360 | 11:19,955,564 | G/A | — | uncertain significance |
| rs2550417019 | 11:19,955,591 | C/A | — | uncertain significance |
| rs372319583 | 11:19,955,609 | G/A | — | uncertain significance |
| rs779400181 | 11:19,955,640 | C/T | — | uncertain significance |
| rs1321120495 | 11:19,955,643 | C/A | — | uncertain significance |
| rs141025466 | 11:19,955,645 | T/C | — | uncertain significance |
| rs139081933 | 11:19,955,670 | C/G | — | uncertain significance |
| rs141668055 | 11:19,955,747 | G/A | — | uncertain significance |
| rs150119037 | 11:19,961,224 | A/C | — | likely benign |
| rs2550500481 | 11:19,961,277 | C/T | — | uncertain significance |
| rs371444762 | 11:19,961,298 | C/A | — | uncertain significance |
| rs901638306 | 11:19,970,251 | C/T | — | uncertain significance |
| rs180786689 | 11:19,970,272 | C/T | — | uncertain significance |
| rs61976957 | 11:19,970,273 | G/A | — | benign |
| rs143426925 | 11:19,970,300 | C/T | — | likely benign |
| rs146729125 | 11:19,970,314 | C/G | — | uncertain significance |
| rs140354139 | 11:19,970,370 | G/A | — | uncertain significance |
| rs759665496 | 11:19,970,379 | A/G | — | uncertain significance |
| rs779752891 | 11:19,970,401 | G/A | — | uncertain significance |
| rs2047153641 | 11:19,970,436 | G/A | — | uncertain significance |
Showing 100 of 240 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.