List of variants in gene CKAP2L reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_152515.5(CKAP2L):c.77A>G (p.Lys26Arg)	rs35593767	0.00324
NM_152515.5(CKAP2L):c.1621A>G (p.Ile541Val)	rs750566749	0.00002
NM_152515.5(CKAP2L):c.1333A>G (p.Thr445Ala)	rs762202417	0.00001
NM_152515.5(CKAP2L):c.1394+3A>G	rs755770296	0.00001
NM_152515.5(CKAP2L):c.907A>G (p.Ile303Val)	rs2104883971

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