Variant (rsID / SNP)
rs4894028
rs4894028 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,403,750. Clinical significance in the table: Benign.
Reference-table entries
TTNBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:179403750
- Cytoband
- 2q31.2
- HGVS
- NM_001267550.2(TTN):c.98912G>A (p.Arg32971His)
- Allele change
- Silent
Associated conditions / phenotypes
Cardiovascular phenotype|Dilated cardiomyopathy 1G|Autosomal recessive limb-girdle muscular dystrophy type 2J|Early-onset myopathy with fatal cardiomyopathy|Myopathy, myofibrillar, 9, with early respiratory failure|Tibial muscular dystrophy|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.