ClinVar Miner

Variants from Language and Genetics Department,Max Planck Institute for Psycholinguistics

Location: Netherlands — 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
4 0 0 0 0 4

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic total
FOXP1 4 4

Condition and significance breakdown #

Total conditions: 1
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Condition pathogenic total
Mental retardation with language impairment and with or without autistic features 4 4

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