ClinVar Miner

Variants studied for Gnb5-related intellectual disability-cardiac arrhythmia syndrome; Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia

Coded as:
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 not provided total
1 0 0 0 0 2 3

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic not provided total
GNB5 1 2 3

Submitter and significance breakdown #

Total submitters: 2
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Submitter pathogenic not provided total
GenomeConnect, ClinGen 0 2 2
Suma Genomics 1 0 1

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