Variant (rsID / SNP)
rs292449
rs292449 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NEDD4L. Location: chromosome 18, position 55,895,081. The table records no clinical significance for this variant.
Reference-table entries
NEDD4LNot classified
- Variant type
- 5_prime_UTR_variant
- Chromosome / position
- 18:55895081
- HGVS
- NM_001144971.2,c.-300G>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.