Variants in gene CEP135 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_025009.5(CEP135):c.2990C>T (p.Ser997Leu)	rs146076380	0.00345
NM_025009.5(CEP135):c.3265T>A (p.Leu1089Ile)	rs76659072	0.00248
NM_025009.5(CEP135):c.1740A>G (p.Arg580=)	rs59759676	0.00155
NM_025009.5(CEP135):c.998AAG[2] (p.Glu335del)	rs374626758

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