Variant (rsID / SNP)
rs3829749
rs3829749 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,395,760. Clinical significance in the table: Benign.
Reference-table entries
TTNBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:179395760
- Cytoband
- 2q31.2
- HGVS
- NM_001267550.2(TTN):c.105582C>T (p.Ser35194_Asp35195=)
- Allele change
- Silent
Associated conditions / phenotypes
Cardiovascular phenotype|Tibial muscular dystrophy|Autosomal recessive limb-girdle muscular dystrophy type 2J|Dilated cardiomyopathy 1G|Early-onset myopathy with fatal cardiomyopathy|Myopathy, myofibrillar, 9, with early respiratory failure|Autosomal recessive limb-girdle muscular dystrophy type 2J|Dilated cardiomyopathy 1G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.