Variant (rsID / SNP)
rs703752
rs703752 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NKX2-5. Location: chromosome 5, position 172,659,511. Clinical significance in the table: Benign.
Reference-table entries
NKX2-5Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:172659511
- Cytoband
- 5q35.1
- HGVS
- NM_004387.4(NKX2-5):c.*61G>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.