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: rs386833897
rs386833897
Entrez Id: 4868;84063
Gene Symbol: NPHS1;KIRREL2
NPHS1;KIRREL2
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
G 0.800 GeneticVariation CLINVAR
dbSNP: rs386833900
rs386833900
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833902
rs386833902
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
C 0.800 GeneticVariation CLINVAR
dbSNP: rs386833905
rs386833905
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
C 0.800 GeneticVariation CLINVAR
dbSNP: rs386833907
rs386833907
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833908
rs386833908
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
G 0.800 GeneticVariation CLINVAR
dbSNP: rs386833911
rs386833911
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833916
rs386833916
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
G 0.800 GeneticVariation CLINVAR
dbSNP: rs386833917
rs386833917
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833929
rs386833929
Entrez Id: 4868;84063
Gene Symbol: NPHS1;KIRREL2
NPHS1;KIRREL2
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
C 0.800 GeneticVariation CLINVAR
dbSNP: rs386833934
rs386833934
Entrez Id: 4868;84063
Gene Symbol: NPHS1;KIRREL2
NPHS1;KIRREL2
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833945
rs386833945
Entrez Id: 4868;84063
Gene Symbol: NPHS1;KIRREL2
NPHS1;KIRREL2
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833946
rs386833946
Entrez Id: 4868;84063
Gene Symbol: NPHS1;KIRREL2
NPHS1;KIRREL2
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.800 GeneticVariation CLINVAR
dbSNP: rs386833949
rs386833949
Entrez Id: 4868;84063
Gene Symbol: NPHS1;KIRREL2
NPHS1;KIRREL2
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.800 GeneticVariation CLINVAR
dbSNP: rs386833960
rs386833960
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs386833961
rs386833961
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 CausalMutation CLINVAR
dbSNP: rs386833961
rs386833961
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
A 0.800 GeneticVariation CLINVAR
dbSNP: rs730880174
rs730880174
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
0.800 GeneticVariation UNIPROT
dbSNP: rs730880174
rs730880174
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
C 0.800 CausalMutation CLINVAR
dbSNP: rs1009762900
rs1009762900
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1054950770
rs1054950770
Entrez Id: 4868;84063
Gene Symbol: NPHS1;KIRREL2
NPHS1;KIRREL2
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516637
rs1057516637
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
TG 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516776
rs1057516776
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516918
rs1057516918
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1057516942
rs1057516942
Entrez Id: 4868;84063
Gene Symbol: NPHS1;KIRREL2
NPHS1;KIRREL2
CUI: C0403399
Disease:
Finnish congenital nephrotic syndrome
C 0.700 GeneticVariation CLINVAR