ClinVar for MedGen (Select 1840935) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3238765	NM_001366145.2(TRPM3):c.4208C>T (p.Pro1403Leu)	KLF9-DT, TRPM3 (P1228L +9 more)	Single nucleotide variant (missense variant +1 more)	Cataract 50 with or without glaucoma	GUncertain significance
Select item 2443699	NM_001366145.2(TRPM3):c.195A>G (p.Ile65Met)	TRPM3 (I67M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance