Variant (rsID / SNP)
rs1071646
rs1071646 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TPM1. Location: chromosome 15, position 63,351,840. Clinical significance in the table: Benign.
Reference-table entries
TPM1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 15:63351840
- Cytoband
- 15q22.2
- HGVS
- NM_001018005.2(TPM1):c.453C>A (p.Ala151=)
- Allele change
- Synonymous_A151A
Associated conditions / phenotypes
Cardiovascular phenotype|Dilated cardiomyopathy 1Y|Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 1|Cardiomyopathy|Hypertrophic cardiomyopathy 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.