C4024664[trait identifier] AND "Centre for Mendelian Genomics, Univers - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 374119	NM_001009944.3(PKD1):c.4846G>T (p.Glu1616Ter)	PKD1 (E1616*)	Single nucleotide variant (nonsense)	3-4 toe syndactyly +3 more	GPathogenic/Likely pathogenic
Select item 523307	NC_012920.1(MT-CO3):m.9355A>T	MT-CO3	Single nucleotide variant	Short stature +12 more	GUncertain significance