Variant (rsID / SNP)
rs186881889
rs186881889 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF1A. Location: chromosome 2, position 241,689,865. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
KIF1AConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:241689865
- Cytoband
- 2q37.3
- HGVS
- NM_001244008.2(KIF1A):c.2958G>C (p.Val986=)
- Allele change
- Synonymous_V894V
Associated conditions / phenotypes
Hereditary spastic paraplegia 30|Neuropathy, hereditary sensory, type 2C|Intellectual disability, autosomal dominant 9|History of neurodevelopmental disorder|Hereditary spastic paraplegia 30|Hereditary spastic paraplegia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.