Variant (rsID / SNP)
rs1716975
rs1716975 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ULK4. Location: chromosome 3, position 41,960,006. Clinical significance in the table: Benign.
Reference-table entries
ULK4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:41960006
- Cytoband
- 3p22.1
- HGVS
- NM_017886.4(ULK4):c.670A>G (p.Ile224Val)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.