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Variant (rsID / SNP)

rs376923877

TNNT2

rs376923877 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNT2. Location: chromosome 1, position 201,328,765. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

TNNT2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:201328765
Cytoband
1q32.1
HGVS
NM_001276345.2(TNNT2):c.837C>T (p.Asn279=)
Allele change
Synonymous_N269N

Associated conditions / phenotypes

Cardiomyopathy|Hypertrophic cardiomyopathy 2|Dilated cardiomyopathy 1D|Cardiomyopathy, familial restrictive, 3

Public references

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