Variant (rsID / SNP)
rs939317
rs939317 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EIF4G1. Location: chromosome 3, position 184,045,799. Clinical significance in the table: Benign.
Reference-table entries
EIF4G1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:184045799
- Cytoband
- 3q27.1
- HGVS
- NM_198241.3(EIF4G1):c.3953+9A>G
- Allele change
- Silent
Associated conditions / phenotypes
Parkinson disease 18, 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.