ClinVar Miner

Variants from Centro de Desenvolvimento Científico e Tecnológico, Secretaria da Saúde do Estado do Rio Grande do Sul

Location: Brazil  Primary collection method: research
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
1 0 0 0 0 1 2

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic not provided total
CFTR 1 0 1
CYP21A2, LOC106780800 0 1 1

Condition and significance breakdown #

Total conditions: 2
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Condition pathogenic not provided total
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency 0 1 1
Cystic fibrosis 1 0 1

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