ClinVar Miner

Variants studied for Centra precocious puberty 1

Coded as:
Minimum submission review status: Collection method:
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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
1 2 1 0 0 4

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
KISS1R 1 2 1 4

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic likely pathogenic uncertain significance total
OMIM 1 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 1 0 1
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 0 0 1 1
National Institute for Research in Reproductive and Child Health, Indian Council of Medical Research 0 1 0 1

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