SNX29
sorting nexin 29
Summary
Predicted to enable phosphatidylinositol binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3851004 | 16:12,071,159 | C/T | — | — |
| rs12922317 | 16:12,077,632 | A/G | intron variant | — |
| rs753855778 | 16:12,096,858 | G/A | — | uncertain significance |
| rs34321532 | 16:12,118,260 | G/A | — | — |
| rs936946964 | 16:12,121,208 | G/A | — | uncertain significance |
| rs181137286 | 16:12,136,759 | G/A | — | uncertain significance |
| rs201192074 | 16:12,136,774 | G/A | — | uncertain significance |
| rs528724487 | 16:12,136,807 | C/T | — | uncertain significance |
| rs571893211 | 16:12,136,822 | C/T | — | uncertain significance |
| rs776441656 | 16:12,136,865 | G/A | — | uncertain significance |
| rs2507000493 | 16:12,136,873 | C/G | — | uncertain significance |
| rs763576162 | 16:12,136,879 | G/A | — | uncertain significance |
| rs1163872987 | 16:12,136,898 | A/G | — | uncertain significance |
| rs140116030 | 16:12,136,906 | A/G | — | uncertain significance |
| rs746914978 | 16:12,136,918 | G/A | — | uncertain significance |
| rs143780467 | 16:12,136,921 | C/T | — | uncertain significance |
| rs1364156092 | 16:12,140,243 | C/T | — | uncertain significance |
| rs146886371 | 16:12,140,287 | A/G | — | uncertain significance |
| rs200133053 | 16:12,142,235 | A/G | — | uncertain significance |
| rs200858924 | 16:12,142,314 | C/G | — | likely benign |
| rs201763407 | 16:12,142,354 | G/C | — | uncertain significance |
| rs746036812 | 16:12,142,378 | C/G | — | uncertain significance |
| rs143274296 | 16:12,142,408 | G/A | — | uncertain significance |
| rs147618832 | 16:12,142,440 | C/T | — | likely benign |
| rs759295478 | 16:12,142,475 | C/T | — | uncertain significance |
| rs777603120 | 16:12,145,725 | G/T | — | uncertain significance |
| rs755260559 | 16:12,145,796 | G/A | — | uncertain significance |
| rs150300274 | 16:12,145,808 | A/T | — | likely benign |
| rs149490127 | 16:12,145,844 | G/A | — | uncertain significance |
| rs201929276 | 16:12,145,847 | C/T | — | uncertain significance |
| rs146360621 | 16:12,145,871 | G/A | — | uncertain significance |
| rs376027540 | 16:12,145,902 | A/G | — | uncertain significance |
| rs2548070030 | 16:12,145,913 | A/G | — | uncertain significance |
| rs144601555 | 16:12,145,950 | A/C | — | uncertain significance |
| rs780627112 | 16:12,145,952 | G/A | — | uncertain significance |
| rs768569593 | 16:12,146,015 | G/A | — | uncertain significance |
| rs554787009 | 16:12,146,019 | A/G | — | uncertain significance |
| rs768785747 | 16:12,146,070 | C/T | — | uncertain significance |
| rs750146655 | 16:12,146,072 | C/T | — | uncertain significance |
| rs190770959 | 16:12,158,574 | C/T | intron variant | — |
| rs8048589 | 16:12,185,810 | T/C | upstream gene variant | — |
| rs350251 | 16:12,202,572 | A/T | — | — |
| rs201891583 | 16:12,223,531 | C/T | — | likely benign |
| rs9673762 | 16:12,230,793 | C/G | intron variant | — |
| rs34098770 | 16:12,237,812 | G/A | intron variant | — |
| rs77986333 | 16:12,334,367 | C/A | — | — |
| rs117147010 | 16:12,596,935 | C/T | intron variant | — |
| rs1641895 | 16:12,641,115 | C/T | regulatory region variant | — |
| rs7195739 | 16:12,648,795 | G/T | — | — |
| rs1171395797 | 16:12,662,393 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.