"IRX5-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3045690	NM_005853.6(IRX5):c.22T>C (p.Leu8=)	IRX5	Single nucleotide variant (synonymous variant)	IRX5-related condition	GLikely benign
Select item 3037463	NM_005853.6(IRX5):c.219C>T (p.Ala73=)	IRX5	Single nucleotide variant (synonymous variant)	IRX5-related condition	GLikely benign
Select item 3053246	NM_005853.6(IRX5):c.549C>T (p.Asn183=)	IRX5, LOC126862355	Single nucleotide variant (synonymous variant)	IRX5-related condition	GLikely benign
Select item 3034152	NM_005853.6(IRX5):c.837G>C (p.Ala279=)	IRX5	Single nucleotide variant (synonymous variant)	IRX5-related condition	GLikely benign
Select item 3050829	NM_005853.6(IRX5):c.987C>A (p.Leu329=)	IRX5	Single nucleotide variant (synonymous variant)	IRX5-related condition	GLikely benign
Select item 745877	NM_005853.6(IRX5):c.1092G>A (p.Gly364=)	IRX5	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3041112	NM_005853.6(IRX5):c.1188G>A (p.Thr396=)	IRX5	Single nucleotide variant (synonymous variant)	IRX5-related condition	GLikely benign
Select item 731657	NM_005853.6(IRX5):c.1203T>G (p.Pro401=)	IRX5	Single nucleotide variant (synonymous variant)	IRX5-related condition +1 more	GLikely benign

ClinVar