ClinVar Miner

Variants studied for Parkinson disease 6, autosomal recessive early-onset

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 not provided total
18 0 13 0 5 2 1 39

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic uncertain significance benign risk factor not provided total
PINK1 18 13 4 0 1 36
MIR6084, PINK1 0 0 1 0 0 1
MT-ND5 0 0 0 1 0 1
MT-ND6 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic uncertain significance benign risk factor not provided total
Invitae 6 8 3 0 0 17
OMIM 12 0 0 2 0 14
Illumina Clinical Services Laboratory,Illumina 1 4 0 0 0 5
Athena Diagnostics Inc 0 0 2 0 0 2
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 1 0 0 0 0 1
Fulgent Genetics,Fulgent Genetics 0 1 0 0 0 1
Centre for Genetic Disorders, Banaras Hindu University 0 0 0 0 1 1

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