ClinVar Miner

Variants studied for Maturity-onset diabetes of the young type 10

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 likely risk allele uncertain risk allele not provided total
4 4 12 4 7 1 2 3 30

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign likely risk allele uncertain risk allele not provided total
INS, INS-IGF2 4 3 11 3 2 1 2 3 22
INS, INS-IGF2, TH 0 0 1 1 5 0 0 0 7
INS 0 1 0 0 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 12
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign likely risk allele uncertain risk allele not provided total
Illumina Laboratory Services, Illumina 0 0 7 4 7 0 0 0 18
Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic 0 0 4 0 0 1 2 0 7
UniProtKB/Swiss-Prot 0 0 0 0 0 0 0 3 3
OMIM 2 0 0 0 0 0 0 0 2
MGZ Medical Genetics Center 0 2 0 0 0 0 0 0 2
Translational Genomics Laboratory, University of Maryland School of Medicine 0 1 0 0 0 0 0 0 1
Medical Genetics, Meyer Children Hospital 0 1 0 0 0 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 1 0 0 0 0 0 0 0 1
Seattle Children's Hospital Molecular Genetics Laboratory, Seattle Children's Hospital 0 1 0 0 0 0 0 0 1
Genome-Nilou Lab 0 0 0 0 1 0 0 0 1
Molecular Genetics, Royal Melbourne Hospital 0 0 1 0 0 0 0 0 1
Shanghai Diabetes Institute, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine 1 0 0 0 0 0 0 0 1

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