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Variant (rsID / SNP)

rs10458896

KIF18A

rs10458896 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF18A. Location: chromosome 11, position 28,057,957. The table records no clinical significance for this variant.

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Reference-table entries

KIF18ANot classified
Variant type
missense_variant
Chromosome / position
11:28057957
HGVS
NM_031217.4,c.2203A>G,p.Ile735Val
Allele change
Missense_I735V

Public references

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