ClinVar Miner

List of variants studied for primary membranoproliferative glomerulonephritis by Centre for Mendelian Genomics, University Medical Centre Ljubljana

Included ClinVar conditions (9):

Basal laminar drusen; Factor H deficiency; Hemolytic uremic syndrome, atypical, susceptibility to, 1; Age related macular degeneration 4
C3 glomerulonephritis
Factor H deficiency
Factor H deficiency; Hemolytic uremic syndrome, atypical, susceptibility to, 1
Hemolytic uremic syndrome, atypical, susceptibility to, 7
Immunoglobulin-mediated membranoproliferative glomerulonephritis
Mesangiocapillary glomerulonephritis
Mesangiocapillary glomerulonephritis, type II
Non-immunoglobulin-mediated membranoproliferative glomerulonephritis

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_003647.3(DGKE):c.966G>A (p.Trp322Ter)	rs138924661	0.00016

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