NPHS1, NPHS1 adhesion molecule, nephrin, 4868

N. diseases: 87; N. variants: 189
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131692245
rs1131692245
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.800 CausalMutation CLINVAR
dbSNP: rs1131692245
rs1131692245
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
0.800 GeneticVariation UNIPROT
dbSNP: rs114203578
rs114203578
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
0.800 GeneticVariation UNIPROT
dbSNP: rs114203578
rs114203578
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
G 0.800 GeneticVariation CLINVAR
dbSNP: rs143092783
rs143092783
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs191807913
rs191807913
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
0.800 GeneticVariation UNIPROT
dbSNP: rs191807913
rs191807913
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.800 GeneticVariation CLINVAR
dbSNP: rs267606917
rs267606917
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
G 0.800 CausalMutation CLINVAR
dbSNP: rs386833861
rs386833861
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.800 GeneticVariation CLINVAR
dbSNP: rs386833862
rs386833862
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.800 GeneticVariation CLINVAR
dbSNP: rs386833864
rs386833864
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
G 0.800 GeneticVariation CLINVAR
dbSNP: rs386833865
rs386833865
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833866
rs386833866
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833867
rs386833867
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833868
rs386833868
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
C 0.800 GeneticVariation CLINVAR
dbSNP: rs386833871
rs386833871
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833875
rs386833875
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833881
rs386833881
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.800 GeneticVariation CLINVAR
dbSNP: rs386833884
rs386833884
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833885
rs386833885
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833886
rs386833886
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833888
rs386833888
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
C 0.800 GeneticVariation CLINVAR
dbSNP: rs386833890
rs386833890
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.800 GeneticVariation CLINVAR
dbSNP: rs386833892
rs386833892
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
C 0.800 GeneticVariation CLINVAR
dbSNP: rs386833894
rs386833894
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.800 GeneticVariation CLINVAR