Variants in gene DEPDC5 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001242896.3(DEPDC5):c.2527C>T (p.Arg843Ter)	rs541024038	0.00001
NM_001242896.3(DEPDC5):c.1474C>T (p.Arg492Ter)	rs1057519107
NM_001242896.3(DEPDC5):c.232del (p.Arg78fs)	rs2082695884
NM_001242896.3(DEPDC5):c.2446C>T (p.Gln816Ter)	rs2148968418
NM_001242896.3(DEPDC5):c.727C>T (p.Arg243Ter)	rs772872014
NM_001242896.3(DEPDC5):c.767+1G>A	rs2148514247

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