ClinVar Miner

Variants from The Division of Genetics and Genomic Medicine,Washington University School of Medicine

Location: United States — 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
2 1 3 0 0 6

Gene and significance breakdown #

Total genes and gene combinations: 4
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
CNTN4 0 0 2 2
DOCK3 2 0 0 2
CNTN4, LOC107522028 0 0 1 1
TCF20 0 1 0 1

Condition and significance breakdown #

Total conditions: 3
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Condition pathogenic likely pathogenic uncertain significance total
Delayed speech and language development 0 0 3 3
Global developmental delay; Muscular hypotonia 2 0 0 2
Autistic behavior; Neurodevelopmental delay; Attention deficit hyperactivity disorder; Muscular hypotonia 0 1 0 1

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