Variants studied for pulmonary hypertension, neonatal, susceptibility to

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
34	83	15	5	2	1	139

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
CPS1	34	83	15	5	2	1	139

Submitter and significance breakdown #

Total submitters: 4

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	risk factor	total
Baylor Genetics	34	80	1	0	0	0	115
Fulgent Genetics, Fulgent Genetics	1	4	14	5	2	0	26
OMIM	0	0	0	0	0	1	1
Division of Human Genetics, Children's Hospital of Philadelphia	0	1	0	0	0	0	1

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