ClinVar Miner

Variants in gene combination COMT, TXNRD2

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 drug response total
0 0 7 1 2 7 16

Condition and significance breakdown #

Total conditions: 5
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Condition uncertain significance likely benign benign drug response total
Primary dilated cardiomyopathy 6 0 0 0 6
Tramadol response 0 0 0 6 6
not provided 2 1 2 0 5
Primary familial hypertrophic cardiomyopathy 1 0 0 0 1
Selective serotonin reuptake inhibitors response - Efficacy 0 0 0 1 1

Submitter and significance breakdown #

Total submitters: 6
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Submitter uncertain significance likely benign benign drug response total
Invitae 6 0 0 0 6
Bruce Budowle Laboratory,University of North Texas Health Science Center 0 0 0 6 6
GeneDx 1 1 2 0 4
Lineagen, Inc 1 0 0 0 1
Blueprint Genetics 1 0 0 0 1
PharmGKB 0 0 0 1 1

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