ClinVar Miner

Variants studied for Bartter syndrome, type 1, antenatal

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
12 4 2 0 1 19

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
SLC12A1 12 4 2 1 19

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance benign total
OMIM 10 0 0 0 10
Fulgent Genetics,Fulgent Genetics 0 0 2 0 2
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 1 1 0 0 2
Athena Diagnostics Inc 0 0 0 1 1
Genomic Research Center,Shahid Beheshti University of Medical Sciences 0 1 0 0 1
Illumina Clinical Services Laboratory,Illumina 0 1 0 0 1
UCLA Clinical Genomics Center, UCLA 1 0 0 0 1
Molecular Diagnostics Laboratory,M Health: University of Minnesota 0 1 0 0 1

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