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Variant (rsID / SNP)

rs3811040

CKAP2L

rs3811040 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CKAP2L. Location: chromosome 2, position 113,498,566. The table records no clinical significance for this variant.

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Reference-table entries

CKAP2LNot classified
Variant type
missense_variant
Chromosome / position
2:113498566
HGVS
NM_152515.5,c.1841T>C,p.Leu614Ser
Allele change
Silent

Public references

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