ClinVar Miner

Variants studied for Menkes kinky-hair syndrome; Cutis laxa, X-linked; X-linked distal spinal muscular atrophy type 3

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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
58 16 544 914 138 1 1655

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
ATP7A 57 16 538 911 136 1 1644
ATP7A, PGK1 0 0 3 3 2 0 7
ATP7A, ATRX, COX7B, MAGT1, PGAM4 1 0 1 0 0 0 2
ATP7A, ATRX, COX7B, MAGT1, PGAM4, PGK1 0 0 1 0 0 0 1
ATP7A, COX7B, MAGT1, PGAM4 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 56 15 535 903 138 0 1647
Natera, Inc. 3 0 6 3 7 0 19
Fulgent Genetics, Fulgent Genetics 0 1 6 4 2 0 13
3billion 0 0 0 8 0 0 8
Juno Genomics, Hangzhou Juno Genomics, Inc 1 0 1 0 0 0 2
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 1 1
New York Genome Center 0 0 1 0 0 0 1

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