Gene entry
SNX29
sorting nexin 29
- Chromosome
- 16
- Cytoband
- 16p13.13-p13.12
- Variants (rsID)
- 184
SNX29 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.13-p13.12). Its official name is “sorting nexin 29”. The reference table lists 184 variants (rsID) for this gene.
Other listed variants
- rs42270
- rs42672
- rs169773
- rs209836
- rs289670
- rs350204
- rs350216
- rs350234
- rs350243
- rs350277
- rs404854
- rs405907
- rs734022
- rs746311
- rs746556
- rs830731
- rs868773
- rs889814
- rs905950
- rs916095
- rs937965
- rs1034391
- rs1035579
- rs1641882
- rs1641894
- rs1641895
- rs2042916
- rs2111225
- rs2430663
- rs2856784
- rs3803604
- rs3851004
- rs3865113
- rs4238614
- rs4780425
- rs4780441
- rs4780452
- rs4781173
- rs4781212
- rs4781218
- rs4781243
- rs4781247
- rs4781251
- rs6498267
- rs7193678
- rs7197059
- rs7198595
- rs7201310
- rs7201595
- rs7203242
- rs7203876
- rs8048589
- rs8052778
- rs8053242
- rs8057488
- rs8062913
- rs8063030
- rs8063329
- rs9921728
- rs9926127
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.