Variant (rsID / SNP)
rs138716837
rs138716837 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLNC. Location: chromosome 7, position 128,481,035. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
FLNCConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:128481035
- Cytoband
- 7q32.1
- HGVS
- NM_001458.5(FLNC):c.1813+11G>T
- Allele change
- Silent
Associated conditions / phenotypes
Hypertrophic cardiomyopathy 26|Myofibrillar myopathy 5|Distal myopathy with posterior leg and anterior hand involvement|Dilated Cardiomyopathy, Dominant
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.