Variant (rsID / SNP)
rs61743870
rs61743870 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LFNG. Location: chromosome 7, position 2,566,484. Clinical significance in the table: Benign.
Reference-table entries
LFNGBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:2566484
- Cytoband
- 7p22.3
- HGVS
- NM_001040167.2(LFNG):c.1002C>T (p.Tyr334=)
- Allele change
- Synonymous_Y263Y
Associated conditions / phenotypes
Spondylocostal dysostosis 3, autosomal recessive
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.