Variant (rsID / SNP)

rs17707385

rs17707385 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF1C. Location: chromosome 17, position 4,904,564. Clinical significance in the table: Benign.

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Reference-table entries

KIF1CBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:4904564
Cytoband: 17p13.2
HGVS: NM_006612.6(KIF1C):c.231T>C (p.Ile77=)
Allele change: Synonymous_I77I

Associated conditions / phenotypes

Spastic ataxia 2

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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