Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs37369
AGXT2
0.807 0.120 5 35037010 missense variant C/T snv 0.21 0.25 9
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs136161
APOL1
0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs2276415
AQP11 ; CLNS1A
0.882 0.160 11 77590296 missense variant G/A snv 0.14 0.13 6
rs121908117
ATRIP ; TREX1 ; ATRIP-TREX1
0.708 0.440 3 48466707 missense variant G/A snv 17
rs739401
CARS1
11 3015094 intron variant C/T snv 0.45 2
rs7947841
CAT
11 34470133 intron variant G/A snv 1.0E-01 1
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs6677604
CFH
0.827 0.200 1 196717788 intron variant G/A snv 0.23 7
rs55807605
CFH
1 196736919 missense variant G/A snv 1.4E-03 5.5E-04 1
rs57960694
CFHR5
1 196994083 missense variant G/A snv 1.1E-02 3.6E-02 1
rs267606743
COL4A1
1.000 0.160 13 110192222 missense variant C/T snv 5
rs1427118369
COL4A3 ; MFF-DT
2 227283830 missense variant G/A snv 4.0E-06 1.4E-05 1
rs121912863
COL4A4
1.000 2 227008112 missense variant G/A snv 1.6E-04 1.8E-04 2
rs868580411
COL4A5
1.000 X 108602973 missense variant G/A;T snv 2
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs4740
EBI3
0.827 0.240 19 4236999 missense variant G/A snv 0.34 0.39 8
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs741301
ELMO1
0.925 0.160 7 36878390 intron variant C/T snv 0.59 3
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36