Variant (rsID / SNP)
rs10497520
rs10497520 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,644,855. Clinical significance in the table: Benign.
Reference-table entries
TTNBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:179644855
- Cytoband
- 2q31.2
- HGVS
- NM_001267550.2(TTN):c.3601A>G (p.Lys1201Glu)
- Allele change
- Missense_K1201E
Associated conditions / phenotypes
Cardiovascular phenotype|Myopathy, myofibrillar, 9, with early respiratory failure|Dilated cardiomyopathy 1G|Early-onset myopathy with fatal cardiomyopathy|Autosomal recessive limb-girdle muscular dystrophy type 2J|Tibial muscular dystrophy|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.