Variants studied for Spermatogenic failure 28; Premature ovarian failure 15

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
0	0	192	31	0	223

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	uncertain significance	likely benign	total
FANCM	187	29	216
FANCM, LOC130055524	5	2	7

Submitter and significance breakdown #

Total submitters: 2

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Submitter	uncertain significance	likely benign	total
Fulgent Genetics, Fulgent Genetics	191	31	222
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago	3	0	3

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