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Variant (rsID / SNP)

rs4561518

KIF2B

rs4561518 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF2B. Location: chromosome 17, position 51,901,643. The table records no clinical significance for this variant.

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Reference-table entries

KIF2BNot classified
Variant type
missense_variant
Chromosome / position
17:51901643
HGVS
NM_032559.5,c.1249C>T,p.Pro417Ser
Allele change
Missense_P417S

Public references

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