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Variant (rsID / SNP)

rs397517781

TTN

rs397517781 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,402,104. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TTNConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:179402104
Cytoband
2q31.2
HGVS
NM_001267550.2(TTN):c.99830G>A (p.Gly33277Glu)
Allele change
Silent

Associated conditions / phenotypes

Dilated Cardiomyopathy, Dominant|Myopathy, myofibrillar, 9, with early respiratory failure|Limb-Girdle Muscular Dystrophy, Recessive|Hypertrophic cardiomyopathy|Early-onset myopathy with fatal cardiomyopathy|Tibial muscular dystrophy|Autosomal recessive limb-girdle muscular dystrophy type 2J|Dilated cardiomyopathy 1G|Cardiomyopathy

Public references

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