Disease: Finnish congenital nephrotic syndrome
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386833945
KIRREL2 ; NPHS1
0.882 0.080 19 35850987 missense variant G/A snv 4
rs386833895
NPHS1
0.925 0.080 19 35845430 missense variant C/A snv 3.6E-05 7.0E-05 2
rs763972372
NPHS1
0.925 0.080 19 35849060 missense variant C/T snv 1.2E-05 2.1E-05 2