List of variants in gene NPHS1 reported as uncertain significance by Athena Diagnostics Inc

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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004646.4(NPHS1):c.697A>G (p.Thr233Ala)	rs35238405	0.00270
NM_004646.4(NPHS1):c.3562G>A (p.Ala1188Thr)	rs116700257	0.00177
NM_004646.4(NPHS1):c.1747G>A (p.Glu583Lys)	rs147641617	0.00059
NM_004646.4(NPHS1):c.1619C>A (p.Ala540Glu)	rs149598144	0.00051
NM_004646.4(NPHS1):c.1850A>G (p.His617Arg)	rs764058957	0.00001
NM_004646.4(NPHS1):c.2054G>A (p.Gly685Asp)	rs1161340572	0.00001
NM_004646.4(NPHS1):c.2159A>C (p.His720Pro)	rs760911714
NM_004646.4(NPHS1):c.2446T>C (p.Cys816Arg)	rs1568453333
NM_004646.4(NPHS1):c.3024A>G (p.Arg1008=)	rs1131691606
NM_004646.4(NPHS1):c.644T>A (p.Leu215Gln)	rs755962215

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.