ClinVar Miner

Variants in gene combination LOC111721705, ZEB2

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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
4 0 6 2 0 12

Condition and significance breakdown #

Total conditions: 4
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Condition pathogenic uncertain significance likely benign total
Mowat-Wilson syndrome 4 2 0 6
not provided 0 3 0 3
not specified 0 1 2 3
History of neurodevelopmental disorder 0 0 1 1

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic uncertain significance likely benign total
Genetic Services Laboratory, University of Chicago 1 1 1 3
Invitae 1 2 0 3
GeneDx 0 1 1 2
OMIM 1 0 0 1
Baylor Miraca Genetics Laboratories, 1 0 0 1
Ambry Genetics 0 0 1 1
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics 0 1 0 1
CeGaT Praxis fuer Humangenetik Tuebingen 0 1 0 1

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