ClinVar for MedGen (Select 934662) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1342270	NM_017583.6(TRIM44):c.*23A>G	TRIM44	Single nucleotide variant (3 prime UTR variant)	Aniridia 3	GBenign
Select item 1342269	NM_017583.6(TRIM44):c.670-27G>C	TRIM44	Single nucleotide variant (intron variant)	Aniridia 3	GBenign
Select item 264710	NM_017583.6(TRIM44):c.463G>A (p.Gly155Arg)	TRIM44 (G155R)	Single nucleotide variant (missense variant)	Aniridia 3	GPathogenic

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