ClinVar Miner

Variants studied for Noonan syndrome 2; Noonan syndrome 10

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
0 3 4 0 0 7

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination likely pathogenic uncertain significance total
LZTR1 3 4 7

Submitter and significance breakdown #

Total submitters: 6
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Submitter likely pathogenic uncertain significance total
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 2 0 2
Center for Molecular Medicine, Children’s Hospital of Fudan University 1 0 1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 1 1
Genetics and Molecular Pathology, SA Pathology 0 1 1
Laboratorio de Biologia Molecular - Genetica, Hospital de Pediatria Garrahan 0 1 1
New York Genome Center 0 1 1

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