"Broad Center for Mendelian Genomics, Broad Institute of MIT and Harva - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 986366	NM_015294.6(TRIM37):c.2243G>A (p.Cys748Tyr)	TRIM37 (C503Y +5 more)	Single nucleotide variant (missense variant +1 more)	Mulibrey nanism syndrome	GUncertain significance
Select item 986367	NM_015294.6(TRIM37):c.934G>A (p.Val312Ile)	TRIM37 (V158I +5 more)	Single nucleotide variant (missense variant +1 more)	Mulibrey nanism syndrome	GUncertain significance