ClinVar Miner

Variants in gene FLT1

See also:
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 70 15 9 7 100

Condition and significance breakdown #

Total conditions: 6
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Condition uncertain significance likely benign benign not provided total
not specified 62 4 0 0 66
not provided 1 10 8 0 19
Carcinoma of colon 1 0 0 7 8
Lung adenocarcinoma 5 0 0 0 5
FLT1-related disorder 0 2 0 0 2
Squamous cell carcinoma 1 0 1 0 2

Submitter and significance breakdown #

Total submitters: 8
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Submitter uncertain significance likely benign benign not provided total
Ambry Genetics 62 4 0 0 66
Labcorp Genetics (formerly Invitae), Labcorp 0 9 7 0 16
Immunobiology Lab; University of Kashmir 1 0 0 7 8
Breakthrough Genomics, Breakthrough Genomics 0 4 4 0 8
Liquid Biopsy and Cancer Interception Group, Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research 6 0 1 0 7
CeGaT Center for Human Genetics Tuebingen 1 3 0 0 4
PreventionGenetics, part of Exact Sciences 0 2 0 0 2
GeneDx 0 0 1 0 1

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