C0206620[trait identifier] AND "Center for Reproductive Medicine, Peki - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 978633	NM_080680.3(COL11A2):c.1773+8T>A	COL11A2	Single nucleotide variant (intron variant)	Heart, malformation of +3 more	GUncertain significance
Select item 497724	NM_080680.3(COL11A2):c.966dup (p.Thr323fs)	COL11A2 (T323fs)	Duplication (frameshift variant +1 more)	Heart, malformation of +8 more	GConflicting classifications of pathogenicity