rs386833895, 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.
Finnish congenital nephrotic syndrome
178 0.925 0.080 19 35845430 missense variant C/A snv 3.6E-05 7.0E-05 0.800 1.000 19 1998 2016
Nephrosis, congenital
CUI: C3501848
Disease: Nephrosis, congenital
9 0.925 0.080 19 35845430 missense variant C/A snv 3.6E-05 7.0E-05 0.010 1.000 1 2018 2018