rs763972372, NPHS1

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Nephrosis, congenital
CUI: C3501848
Disease: Nephrosis, congenital
9 0.925 0.080 19 35849060 missense variant C/T snv 1.2E-05 2.1E-05 0.010 1.000 1 2015 2015
Finnish congenital nephrotic syndrome
178 0.925 0.080 19 35849060 missense variant C/T snv 1.2E-05 2.1E-05 0.700 1.000 6 2005 2017