ClinVar Miner

Variants studied for Focal segmental glomerulosclerosis 4, susceptibility to

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 likely risk allele risk factor total
0 0 7 11 0 1 4 22

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination uncertain significance likely benign likely risk allele risk factor total
APOL1 7 11 1 4 22

Submitter and significance breakdown #

Total submitters: 6
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Submitter uncertain significance likely benign likely risk allele risk factor total
Fulgent Genetics, Fulgent Genetics 5 11 0 0 16
Molecular Diagnostics Lab, Nemours Children's Health, Delaware 0 0 0 3 3
OMIM 0 0 0 2 2
Baylor Genetics 1 0 0 0 1
Mendelics 0 0 1 0 1
Al Jalila Children's Genomics Center, Al Jalila Childrens Speciality Hospital 1 0 0 0 1

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