Gene entry
FMN2
formin 2
- Chromosome
- 1
- Cytoband
- 1q43
- Variants (rsID)
- 95
FMN2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q43). Its official name is “formin 2”. The reference table lists 95 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs146874723Likely benignsingle nucleotide variant
- rs114291166Not classifiedmissense_variant
- rs3795677Not classifiedmissense_variant
Other listed variants
- rs1037666
- rs1414657
- rs1418049
- rs1539200
- rs1572417
- rs2124724
- rs2124728
- rs2152556
- rs3765588
- rs6429194
- rs6658239
- rs6659900
- rs6660298
- rs6664970
- rs6690616
- rs6690640
- rs6699880
- rs7519158
- rs7531340
- rs7544775
- rs7545302
- rs9287233
- rs9287237
- rs9287243
- rs9659428
- rs9728292
- rs9728609
- rs9729181
- rs10495461
- rs10495462
- rs10754695
- rs10754697
- rs10802866
- rs10802870
- rs10926125
- rs10926138
- rs10926147
- rs10926188
- rs10926222
- rs11588029
- rs11590081
- rs11810574
- rs12062492
- rs12064380
- rs12064827
- rs12130718
- rs12131956
- rs12403346
- rs12410581
- rs12723298
- rs12723947
- rs16839692
- rs16840162
- rs17631892
- rs17669357
- rs17672135
- rs17681011
- rs35136065
- rs35361643
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.