Variant (rsID / SNP)
rs2075624
rs2075624 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IVD. Location: chromosome 15, position 40,710,723. Clinical significance in the table: Benign.
Reference-table entries
IVDBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 15:40710723
- Cytoband
- 15q15.1
- HGVS
- NM_002225.5(IVD):c.*261G>A
- Allele change
- Silent
Associated conditions / phenotypes
Isovaleryl-CoA dehydrogenase deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.