ClinVar Miner

Variants studied for Lissencephaly 2; Epilepsy, familial temporal lobe, 7

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 not provided total
0 0 144 64 55 1 264

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination uncertain significance likely benign benign not provided total
RELN 116 53 45 1 215
LOC101927870, RELN 28 11 10 0 49

Submitter and significance breakdown #

Total submitters: 3
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Submitter uncertain significance likely benign benign not provided total
Invitae 144 64 55 0 263
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 1 0 0 0 1
GenomeConnect, ClinGen 0 0 0 1 1

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