Variant (rsID / SNP)

rs4414678

rs4414678 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF1A. Location: chromosome 2, position 241,680,633. 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: 2:241680633
Cytoband: 2q37.3
HGVS: NM_001244008.2(KIF1A):c.3749+53C>A
Allele change: Silent

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.