Variant (rsID / SNP)
rs199694744
rs199694744 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNA1C. Location: chromosome 12, position 2,800,292. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
CACNA1CConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:2800292
- Cytoband
- 12p13.33
- HGVS
- NM_000719.7(CACNA1C):c.6344G>C (p.Gly2115Ala)
- Allele change
- Missense_G2135A
Associated conditions / phenotypes
Cardiovascular phenotype|Long QT syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.