"PreventionGenetics, part of Exact Sciences"[submitter] AND "EPHX2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059509	NM_001979.6(EPHX2):c.164A>G (p.Lys55Arg)	EPHX2 (K2R +1 more)	Single nucleotide variant (missense variant +2 more)	EPHX2-related disorder	GBenign
Select item 3056563	NM_001979.6(EPHX2):c.266A>G (p.Lys89Arg)	EPHX2 (K23R +2 more)	Single nucleotide variant (missense variant +1 more)	EPHX2-related disorder	GBenign
Select item 3043879	NM_001979.6(EPHX2):c.674C>T (p.Pro225Leu)	EPHX2 (P225L +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	EPHX2-related disorder	GLikely benign
Select item 3040006	NM_001979.6(EPHX2):c.810T>C (p.Ser270=)	EPHX2	Single nucleotide variant (synonymous variant +2 more)	EPHX2-related disorder	GLikely benign
Select item 3045333	NM_001979.6(EPHX2):c.909C>T (p.Pro303=)	EPHX2	Single nucleotide variant (synonymous variant +1 more)	EPHX2-related disorder	GLikely benign
Select item 3058383	NM_001979.6(EPHX2):c.1081C>T (p.Pro361Ser)	EPHX2 (P295S +4 more)	Single nucleotide variant (missense variant +1 more)	EPHX2-related disorder	GBenign
Select item 3060428	NM_001979.6(EPHX2):c.1236C>T (p.Ser412=)	EPHX2	Single nucleotide variant (synonymous variant +1 more)	EPHX2-related disorder	GBenign
Select item 3055553	NM_001979.6(EPHX2):c.1275G>A (p.Ala425=)	EPHX2	Single nucleotide variant (synonymous variant +1 more)	EPHX2-related disorder	GBenign

ClinVar