Variants studied for Hyperinsulinemic hypoglycemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)

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
0	12	19	24	16	71

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	likely pathogenic	uncertain significance	likely benign	benign	total
HADH	12	17	18	12	59
HADH, LOC129992931	0	2	6	2	10
KCNJ11	0	0	0	2	2

Submitter and significance breakdown #

Total submitters: 2

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Submitter	likely pathogenic	uncertain significance	likely benign	benign	total
Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic	12	19	24	15	70
Molecular Genetics, Royal Melbourne Hospital	0	0	0	1	1

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