ClinVar Miner

Variants from Clinical Pharmacogenetics Implementation Consortium

Location: United States — Primary collection method: curation
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 0 0 0 591 591

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination drug response total
CYP2C19 405 405
CYP2C19, LOC110599570 186 186

Condition and significance breakdown #

Total conditions: 10
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Condition drug response total
Citalopram response 591 591
Escitalopram response 591 591
Sertraline response 591 591
Voriconazole response 591 591
Clopidogrel response 53 53
CYP2C19: no function 11 11
CYP2C19: uncertain function 10 10
CYP2C19: decreased function 6 6
CYP2C19: normal function 6 6
CYP2C19: increased function 1 1

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