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
rs35138315
COL4A4
0.882 0.200 2 227052367 stop gained G/C snv 6.8E-05 1.1E-04 3
rs375290088
MFF-DT ; COL4A3
0.925 0.120 2 227303904 missense variant G/A snv 8.0E-06 1.4E-05 2
rs35423326
KIRREL2 ; NPHS1
1.000 0.120 19 35861122 missense variant G/A snv 2.9E-02 3.0E-02 1
rs1269093075
MFF-DT ; COL4A3
1.000 0.120 2 227253324 missense variant A/G snv 7.0E-06 1
rs1308023279
MFF-DT ; COL4A3
1.000 0.120 2 227280483 missense variant G/C snv 1.4E-05 1
rs138545216
NPHS2
1.000 0.120 1 179557094 missense variant C/T snv 4.0E-05 1.0E-04 1