ClinVar Miner

Variants studied for Multiple endocrine neoplasia

Coded as:
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 0 103 64 14 178

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination uncertain significance likely benign benign total
RET 54 31 5 88
CDKN1B 16 18 6 40
MEN1 24 9 1 33
CDKN1B, GPR19 6 5 1 12
LOC106736614, RET 3 1 1 5

Submitter and significance breakdown #

Total submitters: 2
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Submitter uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 102 64 10 176
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia 1 0 4 5

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