ClinVar Miner

Variants from Genetics of Infertility and Preimplantation Genetic Diagnosis,Centre Hospitalier Universitaire Grenoble Alpes

Location: France — Primary collection method: case-control
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 total
6 0 0 0 0 6

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic total
ARMC2 5 5
WDR66 1 1

Condition and significance breakdown #

Total conditions: 3
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Condition pathogenic total
Male infertility with teratozoospermia due to single gene mutation 5 5
Sperm tail anomaly 1 1

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