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
36 0 0 0 0 36

Gene and significance breakdown #

Total genes and gene combinations: 27
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Gene or gene combination pathogenic total
ARMC2 5 5
CCDC146 3 3
DMC1 2 2
HENMT1 2 2
TDRD9 2 2
C14orf39 1 1
CFAP206 1 1
CFAP251, LOC124849266 1 1
CFAP91 1 1
CFAP91, LOC129937328 1 1
DDX25 1 1
FAHD1, MEIOB 1 1
FANCM 1 1
GCNA 1 1
HFM1 1 1
IFT74 1 1
KASH5 1 1
MCM8 1 1
MCMDC2 1 1
MNS1 1 1
MNS1, TEX9 1 1
MOV10L1 1 1
MSH5, MSH5-SAPCD1 1 1
PDHA2 1 1
REC8 1 1
TDRKH 1 1
TERB1 1 1

Condition and significance breakdown #

Total conditions: 8
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Condition pathogenic total
Azoospermia 21 21
Male infertility with teratozoospermia due to single gene mutation 7 7
Abnormal sperm tail morphology 2 2
Heterotaxy, visceral, 9, autosomal, with male infertility 2 2
Male infertility due to sperm motility disorder 2 2
Male infertility with spermatogenesis disorder due to single gene mutation 2 2
Multiple Morphological Anomalies of Sperm Flagella (MMAF) 1 1
Spermatogenic failure 18 1 1

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