Variants in gene NRP1 - 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	total
0	0	159	102	17	274

Condition and significance breakdown #

Total conditions: 3

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Condition	uncertain significance	likely benign	benign	total
NRP1-related disorder	110	96	15	221
not specified	66	2	0	68
not provided	1	7	6	13

Submitter and significance breakdown #

Total submitters: 6

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Submitter	uncertain significance	likely benign	benign	total
PreventionGenetics, part of Exact Sciences	110	96	15	221
Ambry Genetics	66	2	0	68
Labcorp Genetics (formerly Invitae), Labcorp	0	3	5	8
Breakthrough Genomics, Breakthrough Genomics	0	1	4	5
CeGaT Center for Human Genetics Tuebingen	0	3	1	4
OMIM	1	0	0	1

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