ClinVar Miner

Variants studied for Diabetes mellitus

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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
22 7 5 0 5 39

Gene and significance breakdown #

Total genes and gene combinations: 11
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
WFS1 7 1 1 3 12
HNF1A 5 3 1 0 9
KCNJ11 5 1 1 0 7
GCK 2 0 0 0 2
GLIS3 0 0 0 2 2
INS, INS-IGF2 0 2 0 0 2
ABCC8 0 0 1 0 1
INS 1 0 0 0 1
KLF11 0 0 1 0 1
RFX6 1 0 0 0 1
SPINK1 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic likely pathogenic uncertain significance benign total
Constantin Polychronakos Laboratory, The Research Institute of the McGill University Health Centre 16 6 3 0 25
Genetic Services Laboratory, University of Chicago 5 1 2 0 8
Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic 1 0 0 5 6
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital 1 0 0 0 1

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