Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs58598099
PKD1
0.882 0.200 16 2116917 missense variant A/G snv 3
rs1131692280
PKD2
0.925 0.120 4 88043458 splice donor variant G/A snv 8.0E-06 1.4E-05 3
rs11122577
AGT
1.000 0.120 1 230711810 intron variant C/A snv 0.19 2
rs1060503526
PKD2
0.925 0.120 4 88038380 stop gained C/T snv 1.2E-05 2
rs121918040
PKD2
0.925 0.120 4 88065479 stop gained C/T snv 7.0E-06 2
rs121918043
PKD2
0.925 0.120 4 88046854 missense variant A/T snv 2
rs1302726543
PKD2
0.925 0.120 4 88019499 stop gained C/T snv 7.0E-06 2
rs1553925453
PKD2
0.925 0.120 4 88038371 missense variant C/T snv 2
rs754868200
PKD2
0.925 0.200 4 88052022 missense variant A/G snv 1.6E-05 7.0E-06 2
rs778235410
PKD2
0.925 0.120 4 88067946 stop gained C/G;T snv 2.4E-05; 1.2E-05 2
rs886041114
PKD2
1.000 0.120 4 88046642 missense variant G/A;T snv 4.0E-06 2
rs1249050389
PTCH1
0.925 0.240 9 95485696 stop gained G/C snv 2
rs1464816
REN
1.000 0.120 1 204159726 intron variant T/C;G snv 2
rs750723025
GANAB ; INTS5
1.000 0.120 11 62646584 inframe deletion TACCGC/- delins 7.0E-06 1
rs1555452849
MIR6511B1 ; PKD1
1.000 0.120 16 2106172 frameshift variant G/- delins 1
rs1187336837
PKD2
1.000 0.120 4 88007931 frameshift variant C/-;CC delins 1