Variant (rsID / SNP)
rs12476289
rs12476289 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,641,975. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
TTNBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:179641975
- Cytoband
- 2q31.2
- HGVS
- NM_001267550.2(TTN):c.4715G>A (p.Arg1572Gln)
- Allele change
- Missense_R1572Q
Associated conditions / phenotypes
Cardiovascular phenotype|Myopathy, myofibrillar, 9, with early respiratory failure|Dilated cardiomyopathy 1G|Early-onset myopathy with fatal cardiomyopathy|Tibial muscular dystrophy|Autosomal recessive limb-girdle muscular dystrophy type 2J|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.