ClinVar Miner

Variants studied for chromosome 15q11.2 deletion syndrome

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
1 1 0 0 0 2

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic total
CCDC92B, CLUH, LOC105371592, MIR1253, MIR6776, PAFAH1B1, RAP1GAP2 0 1 1

Submitter and significance breakdown #

Total submitters: 2
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Submitter pathogenic likely pathogenic total
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 1 1
Centro Nacional de Genética Medica "Dr. Eduardo E. Castilla",Administración Nacional de Laboratorios e Institutos de Salud 1 0 1

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