rs386833912
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
T |
0.800 |
CausalMutation |
CLINVAR |
Treatment and outcome of congenital nephrotic syndrome.
|
29474669 |
2019 |
rs138656762
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs138656762
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
A |
0.800 |
CausalMutation |
CLINVAR |
Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome.
|
27019444 |
2016 |
rs139598219
|
NPHS1;KIRREL2
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs142008044
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs143092783
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs267606917
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833861
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833862
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833863
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833864
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833865
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833866
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833867
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833868
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833871
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833874
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833875
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833879
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833879
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
T |
0.800 |
GeneticVariation |
CLINVAR |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833880
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833881
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833884
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833885
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |
rs386833886
|
Entrez Id: |
4868 |
Gene Symbol: |
NPHS1 |
NPHS1
|
Finnish congenital nephrotic syndrome
|
|
0.800 |
GeneticVariation |
UNIPROT |
NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
|
26560236 |
2016 |