Variant (rsID / SNP)
rs369897647
rs369897647 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEXN. Location: chromosome 1, position 78,398,978. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
NEXNBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:78398978
- Cytoband
- 1p31.1
- HGVS
- NM_144573.4(NEXN):c.1065T>C (p.Asp355=)
- Allele change
- Synonymous_D355D
Associated conditions / phenotypes
Cardiomyopathy|Hypertrophic cardiomyopathy 20|Dilated cardiomyopathy 1CC
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.