Variant (rsID / SNP)
rs141124755
rs141124755 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANK2. Location: chromosome 4, position 114,294,471. Clinical significance in the table: Likely benign.
Reference-table entries
ANK2Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:114294471
- Cytoband
- 4q26
- HGVS
- NM_001148.6(ANK2):c.11725T>C (p.Ser3909Pro)
- Allele change
- Missense_S1753P
Associated conditions / phenotypes
Long QT syndrome|Cardiac arrhythmia, ankyrin-B-related
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.