ClinVar Miner

List of variants in gene combination DM1, DMPK, LOC107075317, LOC129929041 reported as likely benign for myotonic dystrophy type 1

Included ClinVar conditions (1):

Steinert myotonic dystrophy syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_004409.5(DMPK):c.1837G>T (p.Ala613Ser)	rs1003871860	0.00001

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