ClinVar Miner

Variants in gene combination DM1, DMPK, LOC107075317, LOC109461477

See also:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
176 0 0 0 14 190

Condition and significance breakdown #

Total conditions: 1
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Condition pathogenic benign total
Steinert myotonic dystrophy syndrome 176 14 190

Submitter and significance breakdown #

Total submitters: 5
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Submitter pathogenic benign total
Institute of Molecular, Cell and Systems Biology, University of Glasgow 143 0 143
Neuromuscular Research,Maastricht University Medical Centre 48 13 61
OMIM 1 0 1
GeneReviews 0 1 1
Department of Genetics,Sultan Qaboos University Hospital, Oman 1 0 1

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