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Variant (rsID / SNP)

rs79466278

TTN

rs79466278 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,621,349. Clinical significance in the table: Benign.

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Reference-table entries

TTNBenign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
2:179621349
Cytoband
2q31.2
HGVS
NM_001267550.2(TTN):c.10854A>C (p.Gln3618His)
Allele change
Silent

Associated conditions / phenotypes

Dilated cardiomyopathy 1G|Autosomal recessive limb-girdle muscular dystrophy type 2J|Tibial muscular dystrophy|Autosomal recessive limb-girdle muscular dystrophy type 2J|Myopathy, myofibrillar, 9, with early respiratory failure|Early-onset myopathy with fatal cardiomyopathy

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.