Gene entry
FMN1
formin 1
- Chromosome
- 15
- Cytoband
- 15q13.3
- Variants (rsID)
- 153
FMN1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q13.3). Its official name is “formin 1”. The reference table lists 153 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs150962800Benignsingle nucleotide variant
- rs147769257Conflicting interpretationssingle nucleotide variant
- rs139446870Likely benignsingle nucleotide variant
- rs76835557Likely benignsingle nucleotide variant
- rs11858145Not classifiedmissense_variant
- rs1399078Not classifiedmissense_variant
Other listed variants
- rs345749
- rs345776
- rs345800
- rs345827
- rs345830
- rs347925
- rs347931
- rs580115
- rs693818
- rs896507
- rs921510
- rs1258726
- rs1258755
- rs1258784
- rs1258791
- rs1567848
- rs1869663
- rs1871362
- rs2037844
- rs2468747
- rs2597094
- rs2619172
- rs3829481
- rs4238562
- rs4350544
- rs4611425
- rs6494692
- rs6494699
- rs6494897
- rs7162655
- rs7168080
- rs7171392
- rs7173247
- rs7180389
- rs7182810
- rs7183344
- rs8027369
- rs8034124
- rs8034555
- rs8037033
- rs8040565
- rs8040873
- rs9806641
- rs10519765
- rs10519766
- rs11072170
- rs11072312
- rs11629580
- rs11632993
- rs11633462
- rs11637012
- rs11637250
- rs11638794
- rs11854241
- rs12101843
- rs12148180
- rs12593223
- rs12595789
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.