Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs188942711
COL4A3 ; MFF-DT
0.763 0.200 2 227253336 missense variant G/A;T snv 2.8E-05; 4.0E-06 9
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs3752462
MYH9
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53 7
rs121908144
BSND
0.882 0.240 1 54999221 missense variant T/C snv 2.0E-05 3
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs104886303
COL4A5
0.851 0.200 X 108695409 missense variant T/G snv 4