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Variant (rsID / SNP)

rs141505676

TNNC1

rs141505676 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNC1. Location: chromosome 3, position 52,485,867. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TNNC1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
3:52485867
Cytoband
3p21.1
HGVS
NM_003280.3(TNNC1):c.210C>T (p.Gly70=)
Allele change
Synonymous_G70G

Associated conditions / phenotypes

Hypertrophic cardiomyopathy 13|Dilated cardiomyopathy 1Z|Hypertrophic cardiomyopathy 13|Dilated cardiomyopathy 1Z|Cardiomyopathy

Public references

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