"PreventionGenetics, part of Exact Sciences"[submitter] AND "HTRA2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1941845	NM_013247.5(HTRA2):c.64G>A (p.Gly22Ser)	HTRA2 (G22S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 726830	NM_013247.5(HTRA2):c.202C>T (p.Pro68Ser)	HTRA2 (P68S)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 337127	NM_013247.5(HTRA2):c.215T>C (p.Leu72Pro)	HTRA2 (L72P)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 337129	NM_013247.5(HTRA2):c.480C>G (p.Ala160=)	HTRA2	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 337132	NM_013247.5(HTRA2):c.627A>G (p.Arg209=)	HTRA2	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 337137	NM_013247.5(HTRA2):c.1155C>T (p.Pro385=)	HTRA2, LOXL3	Single nucleotide variant (synonymous variant +3 more)	not provided +2 more	GLikely benign
Select item 3032948	NM_013247.5(HTRA2):c.1182T>C (p.His394=)	HTRA2, LOXL3	Single nucleotide variant (synonymous variant +3 more)	HTRA2-related disorder	GLikely benign
Select item 3039120	NM_013247.5(HTRA2):c.1362T>A (p.Pro454=)	HTRA2, LOXL3	Single nucleotide variant (synonymous variant +2 more)	HTRA2-related disorder	GLikely benign

ClinVar