Variant (rsID / SNP)
rs2303602
rs2303602 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DYSF. Location: chromosome 2, position 71,826,102. Clinical significance in the table: Benign.
Reference-table entries
DYSFBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:71826102
- Cytoband
- 2p13.2
- HGVS
- NM_001130987.2(DYSF):c.3756+227C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.