ClinVar Miner

Variants in gene combination MIR6795, NOTCH3

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 total
0 0 0 1 0 1

Condition and significance breakdown #

Total conditions: 1
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Condition likely benign total
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy 1 1

Submitter and significance breakdown #

Total submitters: 1
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Submitter likely benign total
Illumina Clinical Services Laboratory,Illumina 1 1

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