Variants studied for Hereditary spherocytosis

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)
		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
4	5	0	0	0	9

Gene and significance breakdown #

Total genes and gene combinations: 4

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Gene or gene combination	pathogenic	likely pathogenic	total
SPTB	2	2	4
ANK1	0	2	2
SPTA1	2	0	2
GPI	0	1	1

Submitter and significance breakdown #

Total submitters: 4

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Submitter	pathogenic	likely pathogenic	total
MVZ Dr. Eberhard & Partner Dortmund	2	2	4
Diagnostic Genetics, Severance Hospital, Yonsei University College of Medicine	0	3	3
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine	1	0	1
Department of Hematology, 303rd Hospital of the People's Liberation Army	1	0	1

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