"PreventionGenetics, part of Exact Sciences"[submitter] AND "PLCE1-AS1 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 260720	NM_016341.4(PLCE1):c.4724G>C (p.Arg1575Pro)	PLCE1, PLCE1-AS1 (R1575P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Nephrotic syndrome, type 3 +3 more	GBenign
Select item 3031934	NM_016341.4(PLCE1):c.4795+8A>G	PLCE1, PLCE1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	PLCE1-related disorder	GLikely benign
Select item 2636945	NM_016341.4(PLCE1):c.4887dup (p.Ala1630fs)	PLCE1, PLCE1-AS1 (A1322fs +2 more)	Duplication (frameshift variant)	PLCE1-related disorder	GLikely pathogenic
Select item 260721	NM_016341.4(PLCE1):c.4902T>C (p.Ala1634=)	PLCE1, PLCE1-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2632883	NM_016341.4(PLCE1):c.5032C>A (p.Pro1678Thr)	PLCE1, PLCE1-AS1 (P1370T +2 more)	Single nucleotide variant (missense variant)	PLCE1-related disorder	GUncertain significance
Select item 260722	NM_016341.4(PLCE1):c.5035+12C>A	PLCE1, PLCE1-AS1	Single nucleotide variant (intron variant)	Nephrotic syndrome, type 3 +2 more	GBenign

ClinVar