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Variant (rsID / SNP)

rs483352833

TNNT2

rs483352833 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNT2. Location: chromosome 1, position 201,332,502. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

TNNT2Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
1:201332502
Cytoband
1q32.1
HGVS
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=)
Allele change
Synonymous_N164N

Associated conditions / phenotypes

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

Public references

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