Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61747728
NPHS2
0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs104886142
COL4A5
0.790 0.280 X 108598793 missense variant G/A snv 8.7E-05 4.7E-05 10
rs188942711
COL4A3 ; MFF-DT
0.763 0.200 2 227253336 missense variant G/A;T snv 2.8E-05; 4.0E-06 9
rs11089788
MYH9
0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs754313620
INF2
0.925 0.080 14 104714452 missense variant T/C;G snv 7.0E-06 2
rs1131692060
COL4A5
1.000 X 108601404 missense variant G/T snv 1
rs756101090
LAMA5
1.000 20 62330867 missense variant G/A snv 4.1E-05 8.4E-05 1