Variants in gene combination NPHP3, NPHP3-ACAD11 with conflicting interpretations reported as "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: 5

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HGVS	dbSNP	gnomAD frequency
NM_153240.5(NPHP3):c.2694-2_2694-1del	rs751527253	0.00026
NM_153240.5(NPHP3):c.958-2A>G	rs780148543	0.00006
NM_153240.5(NPHP3):c.1174C>T (p.Arg392Ter)	rs1485445500	0.00001
NM_153240.5(NPHP3):c.406del (p.Thr136fs)	rs1379989124
NM_153240.5(NPHP3):c.634dup (p.Glu212fs)	rs747052534

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