ClinVar Miner

Variants studied for Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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
28 7 882 581 65 1 1539

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
WNK1 28 7 879 581 65 1 1536
LOC130007151, WNK1 0 0 2 0 0 0 2
LOC130007151, LOC130007152, WNK1 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 3
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Invitae 28 7 867 566 65 0 1533
Fulgent Genetics, Fulgent Genetics 1 0 109 60 6 0 176
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 1 1

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