Variant (rsID / SNP)
rs149641783
rs149641783 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLNC. Location: chromosome 7, position 128,486,412. 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
- 7:128486412
- Cytoband
- 7q32.1
- HGVS
- NM_001458.5(FLNC):c.4022G>A (p.Arg1341Gln)
- Allele change
- Missense_R1341Q
Associated conditions / phenotypes
Dilated Cardiomyopathy, Dominant|Myofibrillar myopathy 5|Distal myopathy with posterior leg and anterior hand involvement|Hypertrophic cardiomyopathy 26
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.