Variants in gene NKAIN2 - 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	not provided	total
1	0	18	1	1	3	24

Condition and significance breakdown #

Total conditions: 5

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Condition	pathogenic	uncertain significance	likely benign	benign	not provided	total
not specified	0	13	0	0	0	13
not provided	0	4	1	1	1	7
See cases	1	1	0	0	0	2
Normal pregnancy	0	0	0	0	1	1
Small for gestational age	0	0	0	0	1	1

Submitter and significance breakdown #

Total submitters: 7

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Submitter	pathogenic	uncertain significance	likely benign	benign	not provided	total
Ambry Genetics	0	13	0	0	0	13
Quest Diagnostics Nichols Institute San Juan Capistrano	0	4	0	0	0	4
Labcorp Genetics (formerly Invitae), Labcorp	0	0	1	1	0	2
Institute of Molecular and Cell Biology, University of Tartu	0	0	0	0	2	2
GeneDx	1	0	0	0	0	1
ISCA Site 6	0	1	0	0	0	1
GenomeConnect, ClinGen	0	0	0	0	1	1

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