Variant (rsID / SNP)
rs121964856
rs121964856 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNT2. Location: chromosome 1, position 201,334,425. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
TNNT2Pathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:201334425
- Cytoband
- 1q32.1
- HGVS
- NM_001276345.2(TNNT2):c.305G>A (p.Arg102Gln)
- Allele change
- Missense_R92Q
Associated conditions / phenotypes
Hypertrophic cardiomyopathy 2|Hypertrophic cardiomyopathy|Cardiovascular phenotype|Dilated cardiomyopathy 1D|Cardiomyopathy, familial restrictive, 3|Hypertrophic cardiomyopathy 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.