ClinVar Miner

Variants studied for Bartter disease type 4a

Included ClinVar conditions (1):
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
9 1 5 0 1 15

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
BSND 9 1 5 1 15

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic uncertain significance benign total
OMIM 8 0 0 0 8
Illumina Clinical Services Laboratory,Illumina 1 1 2 0 4
Baylor-Hopkins Center for Mendelian Genomics,Johns Hopkins University 0 0 2 0 2
Athena Diagnostics Inc 0 0 0 1 1
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 0 0 1 0 1
Felix Claverie-Martin Laboratory,Hospital Universitario Nuestra Senora de Candelaria 1 0 0 0 1

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