Gene entry
FNBP1
formin binding protein 1
- Chromosome
- 9
- Cytoband
- 9q34.11
- Variants (rsID)
- 38
FNBP1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q34.11). Its official name is “formin binding protein 1”. The reference table lists 38 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs1023000Not classifiedmissense_variant
Other listed variants
- rs484909
- rs2417201
- rs3739861
- rs6478939
- rs7022081
- rs7022657
- rs7870884
- rs10988573
- rs11793428
- rs11794695
- rs13295392
- rs16931713
- rs17519205
- rs35732246
- rs41279162
- rs41304844
- rs41367050
- rs57755031
- rs62583655
- rs72757236
- rs73672538
- rs75213728
- rs75945766
- rs77988508
- rs78668205
- rs78842928
- rs79527131
- rs79919875
- rs111517692
- rs112757767
- rs115197364
- rs117411055
- rs117696636
- rs143944162
- rs183274057
- rs192340914
- rs200931872
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.