List of variants in gene CEP85L reported as pathogenic for Lissencephaly 10

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001042475.3(CEP85L):c.193G>A (p.Asp65Asn)	rs1774229245
NM_001042475.3(CEP85L):c.203T>C (p.Ile68Thr)	rs1774228957
NM_001042475.3(CEP85L):c.232+3G>T	rs754052089
NM_001042475.3(CEP85L):c.232+5G>A	rs1774226763

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