ClinVar Miner

Variants from Service de genetique medicale, Pr. Levy, Hopital de La Timone Enfants, APHM

Location: France  Primary collection method: clinical testing
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
1 4 0 0 0 5

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic total
GAN 0 2 2
FGD4 0 1 1
GDAP1 1 0 1
LRSAM1 0 1 1

Condition and significance breakdown #

Total conditions: 4
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Condition pathogenic likely pathogenic total
Giant axonal neuropathy 1 0 2 2
Charcot-Marie-Tooth disease axonal type 2P 0 1 1
Charcot-Marie-Tooth disease type 4A 1 0 1
Charcot-Marie-Tooth disease type 4H 0 1 1

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