Variants in gene CERKL with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 5

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HGVS	dbSNP	gnomAD frequency
NM_201548.5(CERKL):c.1160-10T>G	rs771126203	0.00016
NM_201548.5(CERKL):c.950G>A (p.Arg317His)	rs150587104	0.00004
NM_201548.5(CERKL):c.953T>C (p.Phe318Ser)	rs745341953	0.00004
NM_201548.5(CERKL):c.356G>A (p.Gly119Asp)	rs1003615909	0.00001
NM_201548.5(CERKL):c.316C>T (p.Arg106Cys)	rs569826109

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