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Variant (rsID / SNP)

rs140003804

TTN

rs140003804 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTN. Location: chromosome 2, position 179,579,035. 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
2:179579035
Cytoband
2q31.2
HGVS
NM_001267550.2(TTN):c.26466C>G (p.Ala8822_Thr8823=)
Allele change
Synonymous_A8505A

Associated conditions / phenotypes

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