List of variants reported as uncertain significance for Nephrotic syndrome by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_016341.4(PLCE1):c.-616_-615dup	rs554480714	0.00021
NM_002292.4(LAMB2):c.3355G>A (p.Gly1119Ser)	rs199570781	0.00011
NM_002292.4(LAMB2):c.3232C>T (p.Arg1078Cys)	rs143284092	0.00006
NM_002292.3(LAMB2):c.-241T>C	rs886058680	0.00004
NM_002292.4(LAMB2):c.4489A>G (p.Lys1497Glu)	rs771769006	0.00001
NM_002292.3(LAMB2):c.-200C>T	rs886058679
NM_002292.3(LAMB2):c.-252T>C	rs886058681
NM_002292.3(LAMB2):c.-279A>T	rs886058682
NM_002292.4(LAMB2):c.2884+15del	rs769133638
NM_016341.4(PLCE1):c.-226del	rs886047492

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.