Variant (rsID / SNP)

rs13411910

rs13411910 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF5C. Location: chromosome 2, position 149,798,512. Clinical significance in the table: Benign.

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Reference-table entries

KIF5CBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:149798512
Cytoband: 2q23.1
HGVS: NM_004522.3(KIF5C):c.501+8G>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.