ClinVar Miner

Variants in gene combination CYP2C19, LOC110599570

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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 other total
0 0 0 0 2 196 1 197

Condition and significance breakdown #

Total conditions: 14
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Condition benign drug response other total
Citalopram response 0 189 0 189
Escitalopram response 0 189 0 189
Sertraline response 0 189 0 189
Voriconazole response 0 189 0 189
Clopidogrel response 0 27 0 27
CYP2C19: normal function 0 2 0 2
CYP2C19: uncertain function 0 2 0 2
CYP2C19: increased function 0 1 0 1
CYP2C19: no function 0 1 0 1
See cases 1 0 0 1
citalopram response - Metabolism/PK 0 1 0 1
clopidogrel response - Dosage, Efficacy, Toxicity/ADR 0 1 0 1
escitalopram response - Metabolism/PK 0 1 0 1
not provided 1 0 1 1

Submitter and significance breakdown #

Total submitters: 4
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Submitter benign drug response other total
Clinical Pharmacogenetics Implementation Consortium 0 195 0 195
GeneDx 2 0 0 2
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics 0 0 1 1
PharmGKB 0 1 0 1

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