Variants studied for Neuropathy, hereditary sensory and autonomic, type 2A; Pseudohypoaldosteronism type 2C

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)

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
38	13	1191	718	66	2	1990

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
WNK1	38	13	1188	718	66	2	1987
LOC130007151, WNK1	0	0	2	0	0	0	2
LOC130007151, LOC130007152, WNK1	0	0	1	0	0	0	1

Submitter and significance breakdown #

Total submitters: 4

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Labcorp Genetics (formerly Invitae), Labcorp	38	11	1051	703	66	0	1869
Fulgent Genetics, Fulgent Genetics	1	3	320	61	6	0	391
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	11	1	0	0	12
GenomeConnect - Invitae Patient Insights Network	0	0	0	0	0	2	2

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