ClinVar Miner

Variants studied for Parkinson disease 8, autosomal dominant

Coded as:
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 risk factor total
15 0 193 46 20 1 236

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign risk factor total
LRRK2 15 193 46 20 1 236

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic uncertain significance likely benign benign risk factor total
GeneReviews 15 127 0 0 0 142
Illumina Clinical Services Laboratory,Illumina 0 49 39 11 0 99
Invitae 2 25 8 9 0 44
OMIM 7 0 0 0 1 8
Courtagen Diagnostics Laboratory,Courtagen Life Sciences 1 0 0 0 0 1
Fulgent Genetics 1 0 0 0 0 1
Institute of Human Genetics,Klinikum rechts der Isar 1 0 0 0 0 1
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 1 0 0 0 0 1

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