ClinVar Miner

Variants studied for Imerslund-Gräsbeck syndrome 1

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
8 0 224 34 85 351

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic uncertain significance likely benign benign total
CUBN 6 223 34 85 348
AMN 2 1 0 0 3

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 219 34 78 331
Nilou-Genome Lab 0 0 0 28 28
Baylor Genetics 0 7 0 0 7
OMIM 6 0 0 0 6
Victorian Clinical Genetics Services,Murdoch Childrens Research Institute 0 2 0 0 2
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 2 0 0 0 2

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