Variant (rsID / SNP)
rs12185268
rs12185268 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPPL2C. Location: chromosome 17, position 43,923,683. The table records no clinical significance for this variant.
Reference-table entries
SPPL2CNot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:43923683
- HGVS
- NM_175882.3,c.1411A>G,p.Ile471Val
- Allele change
- Silent
Associated conditions / phenotypes
Multiple System Atrophy 1|Parkinson Disease, Late-Onset|Rem Sleep Behavior Disorder|Fainting|Autonomic Dysfunction|Head Injury
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.