NPHS2, NPHS2 stomatin family member, podocin, 7827

N. diseases: 86; N. variants: 67
Disease: Nephrotic range proteinuria ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs74315342
rs74315342
Entrez Id: 7827
Gene Symbol: NPHS2
NPHS2
CUI: C0445118
Disease:
Nephrotic range proteinuria 		T 0.700 CausalMutation CLINVAR
dbSNP: rs749740335
rs749740335
Entrez Id: 7827;126859
Gene Symbol: NPHS2;AXDND1
NPHS2;AXDND1
CUI: C0445118
Disease:
Nephrotic range proteinuria 		C 0.700 CausalMutation CLINVAR