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Variant (rsID / SNP)

rs727505233

TNNT2

rs727505233 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNT2. Location: chromosome 1, position 201,328,369. Clinical significance in the table: Uncertain significance.

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Reference-table entries

TNNT2Uncertain significance
Clinical significance (as recorded)
Uncertain significance
Variant type
single nucleotide variant
Chromosome / position
1:201328369
Cytoband
1q32.1
HGVS
NM_001276345.2(TNNT2):c.866G>A (p.Gly289Glu)
Allele change
Missense_G279E

Associated conditions / phenotypes

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.