Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4972593
LOC107985961
0.925 0.200 2 173598126 intergenic variant T/A snv 0.20 3
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs4821480
MYH9
0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs2228226
GLI1 ; ARHGAP9
0.851 0.160 12 57472038 missense variant G/C snv 0.60 0.68 6
rs121918673
HNF1B
0.925 0.200 17 37701122 missense variant G/C snv 1.9E-05 3
rs136161
APOL1
0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs2234584
WT1
0.882 0.240 11 32428521 missense variant G/A;T snv 3.9E-04; 2.8E-05 5
rs55703767
MFF-DT ; COL4A3
0.925 0.160 2 227256385 missense variant G/A;T snv 4.0E-06; 0.17 3
rs868580411
COL4A5
1.000 X 108602973 missense variant G/A;T snv 2
rs13293564
UNC13B
9 35166766 intron variant G/A;T snv 1
rs9357155
PSMB8
1.000 0.120 6 32842071 non coding transcript exon variant G/A;C snv 2
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs121908117
ATRIP ; TREX1 ; ATRIP-TREX1
0.708 0.440 3 48466707 missense variant G/A snv 17
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14
rs74421874
PSMD9
0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14