ClinVar Miner

Variants studied for Rabson-Mendenhall syndrome

Included ClinVar conditions (2):
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
8 0 152 28 63 250

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign total
INSR 8 152 28 63 250

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 148 28 63 239
OMIM 4 0 0 0 4
Fulgent Genetics,Fulgent Genetics 0 4 0 0 4
Medical Research Institute,Tokyo Medical and Dental University 2 0 0 0 2
Laboratory of Molecular Biology and Genetics,St Antoine Hospital - APHP 1 0 0 0 1
The Translational Medicine Center of Children Development and Disease,Fudan University 1 0 0 0 1

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