ClinVar Miner

List of variants in gene combination DM1, DMPK, LOC107075317, LOC109461477, LOC129929040 reported as 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004409.4(DMPK):c.*224CTG[(35_49)]
NM_004409.5(DMPK):c.*224CTG[1]
NM_004409.5(DMPK):c.224_283=

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