ClinVar Miner

Variants studied for Rh deficiency syndrome

Included ClinVar conditions (4):
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
12 1 0 0 1 1 14

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic benign not provided total
RHAG 12 1 1 1 14

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic benign not provided total
OMIM 12 0 0 0 12
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 1 0 0 2
Fulgent Genetics, Fulgent Genetics 0 0 1 0 1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center 0 0 1 0 1
GenomeConnect, ClinGen 0 0 0 1 1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 0 0 1 0 1

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