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
147 0 0 0 1 148

Condition and significance breakdown #

Total conditions: 1
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Condition pathogenic benign total
Steinert myotonic dystrophy syndrome 147 1 148

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic benign total
Institute of Molecular, Cell and Systems Biology, University of Glasgow 145 0 145
OMIM 1 0 1
GeneReviews 0 1 1
Department of Genetics,Sultan Qaboos University Hospital, Oman 1 0 1

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