ClinVar Miner

Variants in gene combination KIRREL2, NPHS1

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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 total
0 4 7 5 3 16

Condition and significance breakdown #

Total conditions: 4
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Condition likely pathogenic uncertain significance likely benign benign total
Finnish congenital nephrotic syndrome 4 5 4 0 12
not specified 0 1 0 3 3
See cases 0 0 1 0 1
not provided 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 9
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Submitter likely pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 3 2 0 5
Counsyl 2 0 2 0 4
PreventionGenetics 0 0 0 3 3
Juha Muilu Group; Institute for Molecular Medicine Finland (FIMM) 2 0 0 0 2
Athena Diagnostics Inc 0 1 0 0 1
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics 0 1 0 0 1
ISCA site 6 0 0 1 0 1
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 0 1 0 0 1
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 0 1 0 0 1

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