Related gene-specific medical variations for Gene (Select 64750) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042354	NM_022739.4(SMURF2):c.-33CCCGCCGCC[2]	LOC130061444, SMURF2	Microsatellite (5 prime UTR variant)	SMURF2-related disorder	GBenign
Select item 2648101	NM_022739.4(SMURF2):c.51A>G (p.Thr17=)	LOC130061444, SMURF2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1173034	NM_022739.4(SMURF2):c.52+5G>A	LOC130061444, SMURF2	Single nucleotide variant (intron variant)	not provided	GUncertain significance

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