Variants from Dunham Lab, University of Washington

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
96	148	17	3	20	284

Gene and significance breakdown #

Total genes and gene combinations: 5

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
G6PD	93	143	16	3	15	270
G6PD, IKBKG	2	4	1	0	2	9
G6PD, IKBKG, LOC107181288	1	0	0	0	1	2
G6PD, IKBKG, LOC108281126	0	0	0	0	2	2
G6PD, IKBKG, LOC107181288, LOC129929052	0	1	0	0	0	1

Condition and significance breakdown #

Total conditions: 1

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Condition	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Anemia, nonspherocytic hemolytic, due to G6PD deficiency	96	148	17	3	20	284

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