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Variant (rsID / SNP)

rs116600932

KIF1A

rs116600932 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF1A. Location: chromosome 2, position 241,689,833. Clinical significance in the table: Benign.

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Reference-table entries

KIF1ABenign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
2:241689833
Cytoband
2q37.3
HGVS
NM_001244008.2(KIF1A):c.2977+13C>T
Allele change
Silent

Associated conditions / phenotypes

Hereditary spastic paraplegia 30|Neuropathy, hereditary sensory, type 2C|Intellectual disability, autosomal dominant 9|Hereditary spastic paraplegia 30

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.