"PreventionGenetics, part of Exact Sciences"[submitter] AND "IVNS1ABP" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2635796	NM_006469.5(IVNS1ABP):c.1675G>C (p.Gly559Arg)	IVNS1ABP (G559R)	Single nucleotide variant (missense variant)	IVNS1ABP-related condition	GUncertain significance
Select item 2629391	NM_006469.5(IVNS1ABP):c.1399A>G (p.Ile467Val)	IVNS1ABP (I467V)	Single nucleotide variant (missense variant)	IVNS1ABP-related condition	GUncertain significance
Select item 3033709	NM_006469.5(IVNS1ABP):c.934T>C (p.Phe312Leu)	IVNS1ABP (F312L)	Single nucleotide variant (missense variant)	IVNS1ABP-related condition	GUncertain significance
Select item 2630013	NM_006469.5(IVNS1ABP):c.379T>C (p.Ser127Pro)	IVNS1ABP (S127P)	Single nucleotide variant (missense variant)	IVNS1ABP-related condition	GUncertain significance
Select item 3047896	NM_006469.5(IVNS1ABP):c.282-7dup	IVNS1ABP	Duplication (intron variant)	IVNS1ABP-related condition	GLikely benign
Select item 3029365	NM_006469.5(IVNS1ABP):c.282-7T>A	IVNS1ABP	Single nucleotide variant (intron variant)	IVNS1ABP-related condition	GLikely benign
Select item 3044440	NM_006469.5(IVNS1ABP):c.240A>G (p.Pro80=)	IVNS1ABP	Single nucleotide variant (synonymous variant)	IVNS1ABP-related condition	GLikely benign

ClinVar