List of variants in gene WT1 reported as likely pathogenic for Nephrotic syndrome, type 4

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:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_024426.6(WT1):c.1259A>C (p.His420Pro)	rs1554939785
NM_024426.6(WT1):c.1268A>G (p.Glu423Gly)	rs2132921573
NM_024426.6(WT1):c.1322A>T (p.Asp441Val)	rs2132920206
NM_024426.6(WT1):c.1367T>G (p.Phe456Cys)	rs2494732361
NM_024426.6(WT1):c.1384C>T (p.Gln462Ter)	rs2132914929
NM_024426.6(WT1):c.1388G>A (p.Arg463Gln)	rs1037084691
NM_024426.6(WT1):c.1394T>C (p.Phe465Ser)	rs2132914663
NM_024426.6(WT1):c.1399C>T (p.Arg467Trp)	rs121907900
NM_024426.6(WT1):c.1400G>A (p.Arg467Gln)	rs121907903
NM_024426.6(WT1):c.1447+4C>T	rs587776577
NM_024426.6(WT1):c.1504G>C (p.Asp502His)	rs2132898667
NM_024426.6(WT1):c.896T>A (p.Leu299Ter)	rs2494370978

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.