Variant (rsID / SNP)

rs3732338

rs3732338 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF1A. Location: chromosome 2, position 241,655,038. 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: 2:241655038
Cytoband: 2q37.3
HGVS: NM_001244008.2(KIF1A):c.*1743G>A
Allele change: Silent

Associated conditions / phenotypes

Hereditary spastic paraplegia 30

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.