ClinVar Miner

Variants studied for immunoglobulin A deficiency 2

Included ClinVar conditions (2):
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
6 3 9 1 0 17

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign total
TNFRSF13B 6 3 9 1 17

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic likely pathogenic uncertain significance likely benign total
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 1 2 3 1 7
Fulgent Genetics, Fulgent Genetics 0 1 5 0 6
OMIM 3 0 0 0 3
Baylor Genetics 2 0 1 0 3
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 1 0 0 0 1
Division of Human Genetics, Children's Hospital of Philadelphia 1 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 1 0 0 0 1
New York Genome Center 0 0 1 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 1 0 1

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