ClinVar Miner

Variants studied for Deafness, autosomal dominant 4b

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 total
3 0 4 0 1 8

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance benign total
CEACAM16 3 4 1 8

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic uncertain significance benign total
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories 0 2 1 3
OMIM 2 0 0 2
Baylor Genetics 0 2 0 2
ColIege of Otolaryngology Head and Neck Surgery,Chinese PLA General Hospital 1 0 0 1

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