Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs386833912
rs386833912
NPHS1
T 0.800 CausalMutation CLINVAR Treatment and outcome of congenital nephrotic syndrome. 29474669

2019
dbSNP: rs138656762
rs138656762
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs138656762
rs138656762
NPHS1
A 0.800 CausalMutation CLINVAR Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome. 27019444

2016
dbSNP: rs139598219
rs139598219
NPHS1 ; KIRREL2
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs142008044
rs142008044
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs143092783
rs143092783
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs267606917
rs267606917
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833861
rs386833861
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833862
rs386833862
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833863
rs386833863
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833864
rs386833864
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833865
rs386833865
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833866
rs386833866
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833867
rs386833867
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833868
rs386833868
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833871
rs386833871
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833874
rs386833874
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833875
rs386833875
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833879
rs386833879
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833879
rs386833879
NPHS1
T 0.800 GeneticVariation CLINVAR NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833880
rs386833880
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833881
rs386833881
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833884
rs386833884
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833885
rs386833885
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016
dbSNP: rs386833886
rs386833886
NPHS1
0.800 GeneticVariation UNIPROT NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described. 26560236

2016