Variant (rsID / SNP)
rs72554080
rs72554080 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GIGYF2. Location: chromosome 2, position 233,612,450. Clinical significance in the table: risk factor.
Reference-table entries
GIGYF2Risk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:233612450
- Cytoband
- 2q37.1
- HGVS
- NM_001103146.3(GIGYF2):c.167A>G (p.Asn56Ser)
- Allele change
- Missense_N56S
Associated conditions / phenotypes
Parkinson disease 11, autosomal dominant, susceptibility to
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.