Variant (rsID / SNP)
rs9636153
rs9636153 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNNI3, TNNT1. Location: chromosome 19, position 55,660,537. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
TNNI3Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:55660537
- Cytoband
- 19q13.42
- HGVS
- NM_003283.6(TNNT1):c.-20A>G
- Allele change
- Silent
Associated conditions / phenotypes
Nemaline Myopathy, Recessive|Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome|Hypertrophic cardiomyopathy|Familial restrictive cardiomyopathy|Dilated Cardiomyopathy, Recessive|Nemaline myopathy 5
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.