Variants in gene CCDC39 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_181426.2(CCDC39):c.1167+1261A>G	rs577069249	0.00051
NM_181426.2(CCDC39):c.610-2A>G	rs756235547	0.00009
NM_181426.2(CCDC39):c.1874G>T (p.Ser625Ile)	rs769223754	0.00006
NM_181426.2(CCDC39):c.1356C>A (p.Tyr452Ter)	rs375839864	0.00001
NM_181426.2(CCDC39):c.1665+1G>A	rs753580394	0.00001
NM_181426.2(CCDC39):c.1045del (p.Thr349fs)	rs747980515
NM_181426.2(CCDC39):c.1484_1485del (p.Lys495fs)	rs751239231
NM_181426.2(CCDC39):c.1871_1872del (p.Ile624fs)	rs1560086701
NM_181426.2(CCDC39):c.2226C>A (p.Tyr742Ter)	rs772219642
NM_181426.2(CCDC39):c.436del (p.Trp146fs)	rs2108429507
NM_181426.2(CCDC39):c.830_831del (p.Thr277fs)	rs773801386

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