Variant (rsID / SNP)

rs397516454

rs397516454 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNT2. Location: chromosome 1, position 201,334,738. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

TNNT2Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:201334738
Cytoband: 1q32.1
HGVS: NM_001276345.2(TNNT2):c.294T>G (p.Asp98Glu)
Allele change: Missense_D88E

Associated conditions / phenotypes

Primary dilated cardiomyopathy

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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