"Illumina Laboratory Services, Illumina"[submitter] AND "ODAD3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 328161	NM_002743.2(PRKCSH):c.-336G>A	ODAD3, PRKCSH	Single nucleotide variant (intron variant)	Polycystic liver disease 1	GBenign
Select item 328162	NM_002743.2(PRKCSH):c.-299_-298CT[1]	ODAD3, PRKCSH	Microsatellite (intron variant)	Polycystic liver disease 1	GLikely benign
Select item 328163	NM_002743.2(PRKCSH):c.-193G>A	ODAD3, PRKCSH	Single nucleotide variant (intron variant)	Polycystic liver disease 1	GUncertain significance
Select item 328164	NM_002743.2(PRKCSH):c.-168G>A	ODAD3, PRKCSH	Single nucleotide variant (intron variant)	Polycystic liver disease 1	GUncertain significance
Select item 328165	NM_001289104.2(PRKCSH):c.-143G>A	ODAD3, PRKCSH	Single nucleotide variant (5 prime UTR variant +1 more)	Polycystic liver disease 1	GLikely benign
Select item 328166	NM_001289104.2(PRKCSH):c.-130C>T	ODAD3, PRKCSH	Single nucleotide variant (5 prime UTR variant +1 more)	Polycystic liver disease 1	GBenign
Select item 328167	NM_001289104.2(PRKCSH):c.-119C>G	ODAD3, PRKCSH	Single nucleotide variant (5 prime UTR variant +1 more)	Polycystic liver disease 1	GBenign
Select item 328168	NM_001289104.2(PRKCSH):c.-105T>C	PRKCSH, ODAD3	Single nucleotide variant (5 prime UTR variant +1 more)	Polycystic liver disease 1	GUncertain significance

ClinVar