Variant (rsID / SNP)
rs2255632
rs2255632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SZT2. Location: chromosome 1, position 43,909,265. Clinical significance in the table: Benign.
Reference-table entries
SZT2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:43909265
- Cytoband
- 1p34.2
- HGVS
- NM_001365999.1(SZT2):c.8626-3T>C
- Allele change
- Silent
Associated conditions / phenotypes
Seizure
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.