Variant (rsID / SNP)
rs72648954
rs72648954 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,593,449. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:179593449
- Cytoband
- 2q31.2
- HGVS
- NM_001267550.2(TTN):c.19204A>G (p.Met6402Val)
- Allele change
- Missense_M6085V
Associated conditions / phenotypes
Cardiovascular phenotype|Dilated cardiomyopathy 1G|Myopathy, myofibrillar, 9, with early respiratory failure|Autosomal recessive limb-girdle muscular dystrophy type 2J|Tibial muscular dystrophy|Early-onset myopathy with fatal cardiomyopathy|Cardiomyopathy|Dilated cardiomyopathy 1G|Autosomal recessive limb-girdle muscular dystrophy type 2J
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.