C3250443[trait identifier] AND "GeneReviews"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 65629	NM_004409.4(DMPK):c.*224CTG[(35_49)]	DM1-AS, DMPK +3 more	Microsatellite	Steinert myotonic dystrophy syndrome	Gother
Select item 65631	Single allele		Microsatellite	Steinert myotonic dystrophy syndrome	GPathogenic
Select item 65630	NM_001081563.1(DMPK):c.224_226CTG[(5-34)]		Microsatellite	Steinert myotonic dystrophy syndrome	GBenign

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