Variants in gene FGF17 - ClinVar Miner

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	risk factor	total
2	0	20	22	12	1	54

Condition and significance breakdown #

Total conditions: 5

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Condition	pathogenic	uncertain significance	likely benign	benign	risk factor	total
not provided	0	9	21	12	0	41
not specified	0	10	0	1	0	11
FGF17-related disorder	0	1	1	0	0	2
Hypogonadotropic hypogonadism 20 with or without anosmia	1	0	0	0	1	2
Hypogonadotropic hypogonadism 20 without anosmia	1	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 8

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Submitter	pathogenic	uncertain significance	likely benign	benign	risk factor	total
Labcorp Genetics (formerly Invitae), Labcorp	0	8	16	6	0	30
GeneDx	0	1	4	7	0	12
Breakthrough Genomics, Breakthrough Genomics	0	0	4	8	0	12
Ambry Genetics	0	10	0	0	0	10
OMIM	2	0	0	0	1	3
PreventionGenetics, part of Exact Sciences	0	1	1	0	0	2
CeGaT Center for Human Genetics Tuebingen	0	0	2	0	0	2
Genetic Services Laboratory, University of Chicago	0	0	0	1	0	1

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