Gene entry
FHIT
fragile histidine triad diadenosine triphosphatase
- Chromosome
- 3
- Cytoband
- 3p14.2
- Variants (rsID)
- 459
FHIT is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p14.2). Its official name is “fragile histidine triad diadenosine triphosphatase”. The reference table lists 459 variants (rsID) for this gene.
Other listed variants
- rs49411
- rs169915
- rs177139
- rs182418
- rs191927
- rs212036
- rs212050
- rs212059
- rs213294
- rs213347
- rs213348
- rs213354
- rs213374
- rs213388
- rs213396
- rs213406
- rs213415
- rs242222
- rs294454
- rs294461
- rs410072
- rs410351
- rs475675
- rs492836
- rs521388
- rs624225
- rs689498
- rs715382
- rs722070
- rs724025
- rs732380
- rs741891
- rs760316
- rs780365
- rs780367
- rs809710
- rs931317
- rs970387
- rs996174
- rs1005463
- rs1006902
- rs1016449
- rs1022445
- rs1026989
- rs1040336
- rs1353545
- rs1385715
- rs1385816
- rs1447958
- rs1496652
- rs1562519
- rs1562521
- rs1562523
- rs1562525
- rs1579912
- rs1597104
- rs1683354
- rs1683366
- rs1716722
- rs1716727
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
