Gene entry
FBN3
fibrillin 3
- Chromosome
- 19
- Cytoband
- 19p13.2
- Variants (rsID)
- 59
FBN3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19p13.2). Its official name is “fibrillin 3”. The reference table lists 59 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs138457751Uncertain significancesingle nucleotide variant
- rs12608849Not classifiedmissense_variantScoliosis|Idiopathic Scoliosis|Scoliosis, Isolated 1
- rs12975322Not classifiedmissense_variant
- rs35025963Not classifiedmissense_variant
- rs4804063Not classifiedmissense_variant
- rs4804264Not classifiedsynonymous_variant
- rs7245429Not classifiedmissense_variant
- rs7257948Not classifiedmissense_variantScoliosis|Idiopathic Scoliosis|Scoliosis, Isolated 1
Other listed variants
- rs3813774
- rs3848570
- rs4527136
- rs6603141
- rs6603148
- rs7245558
- rs7247560
- rs7257658
- rs8103218
- rs10906992
- rs11260062
- rs12162233
- rs12986396
- rs17160134
- rs17160149
- rs17160196
- rs33967815
- rs34744486
- rs35277492
- rs35318692
- rs35579498
- rs36124795
- rs61729599
- rs61729609
- rs61735544
- rs72993518
- rs73003698
- rs76318007
- rs78908341
- rs111332402
- rs115491028
- rs118050938
- rs138756263
- rs139075860
- rs139787266
- rs141592778
- rs142789080
- rs144789622
- rs146679363
- rs146977165
- rs147206351
- rs147683023
- rs148428757
- rs149073155
- rs149496112
- rs149549572
- rs149936210
- rs181718091
- rs182123827
- rs201729752
- rs201873196
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.