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Variant (rsID / SNP)

rs35593767

CKAP2L

rs35593767 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CKAP2L. Location: chromosome 2, position 113,520,107. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CKAP2LConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:113520107
Cytoband
2q14.1
HGVS
NM_152515.5(CKAP2L):c.77A>G (p.Lys26Arg)
Allele change
Silent

Public references

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