Variants from Clingen PTEN Variant Curation Expert Panel, Clingen

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
60	45	58	31	10	204

Gene and significance breakdown #

Total genes and gene combinations: 4

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
PTEN	60	45	49	22	7	183
KLLN, LOC130004273, PTEN	0	0	1	4	2	7
KLLN, PTEN	0	0	3	3	1	7
LOC130004273, PTEN	0	0	5	2	0	7

Condition and significance breakdown #

Total conditions: 1

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Condition	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
PTEN hamartoma tumor syndrome	60	45	58	31	10	204

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