Variant (rsID / SNP)
rs3744124
rs3744124 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLCN. Location: chromosome 17, position 17,124,815. Clinical significance in the table: Benign.
Reference-table entries
FLCNBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:17124815
- Cytoband
- 17p11.2
- HGVS
- NM_144997.7(FLCN):c.871+36G>A
- Allele change
- Silent
Associated conditions / phenotypes
Multiple fibrofolliculomas
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.