"PreventionGenetics, part of Exact Sciences"[submitter] AND "MEOX1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 714734	NM_004527.4(MEOX1):c.713A>G (p.Asn238Ser)	MEOX1 (N123S +1 more)	Single nucleotide variant (missense variant +1 more)	MEOX1-related disorder +1 more	GLikely benign
Select item 736085	NM_004527.4(MEOX1):c.700C>A (p.Pro234Thr)	MEOX1 (A176D +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3029888	NM_004527.4(MEOX1):c.165G>A (p.Ala55=)	MEOX1	Single nucleotide variant (5 prime UTR variant +1 more)	MEOX1-related disorder	GLikely benign
Select item 259424	NM_004527.4(MEOX1):c.80C>T (p.Ser27Leu)	MEOX1 (S27L)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 259423	NM_004527.4(MEOX1):c.11C>T (p.Ala4Val)	MEOX1 (A4V)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GBenign
Select item 3053455	NM_004527.4(MEOX1):c.-9G>A	MEOX1	Single nucleotide variant (5 prime UTR variant +1 more)	MEOX1-related disorder	GLikely benign

ClinVar