ClinVar Miner

Variants in gene combination FLT1, LOC126861720

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 6 1 0 3 10

Condition and significance breakdown #

Total conditions: 3
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Condition uncertain significance likely benign not provided total
not specified 6 0 0 6
Carcinoma of colon 0 0 3 3
not provided 0 1 0 1

Submitter and significance breakdown #

Total submitters: 5
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Submitter uncertain significance likely benign not provided total
Ambry Genetics 6 0 0 6
Immunobiology Lab; University of Kashmir 0 0 3 3
Labcorp Genetics (formerly Invitae), Labcorp 0 1 0 1
CeGaT Center for Human Genetics Tuebingen 0 1 0 1
Breakthrough Genomics, Breakthrough Genomics 0 1 0 1

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