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Variant (rsID / SNP)

rs17350674

KIF24

rs17350674 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF24. Location: chromosome 9, position 34,306,410. The table records no clinical significance for this variant.

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Reference-table entries

KIF24Not classified
Variant type
missense_variant
Chromosome / position
9:34306410
HGVS
NM_194313.4,c.653G>T,p.Trp218Leu
Allele change
Missense_W218L

Associated conditions / phenotypes

Aphasia|Amyotrophic Lateral Sclerosis 12 with or Without Frontotemporal Dementia|Frontotemporal Dementia|Semantic Dementia

Public references

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