"GeneReviews"[submitter] AND "MSTN"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 65688	NM_005259.3(MSTN):c.458A>G (p.Lys153Arg)	C2orf88, MSTN (K153R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 7705	NM_005259.3(MSTN):c.373+5G>A	C2orf88, MSTN	Single nucleotide variant (intron variant)	Myostatin-related muscle hypertrophy	GPathogenic
Select item 65687	NM_005259.3(MSTN):c.163G>A (p.Ala55Thr)	C2orf88, MSTN (A55T)	Single nucleotide variant (missense variant)	Myostatin-related muscle hypertrophy +1 more	GBenign

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