Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1866813 1.000 0.120 3 137083096 intergenic variant A/C snv 0.14 1
rs304029
ITPR1
1.000 0.120 3 4504140 intron variant A/C snv 0.35 1
rs334543 1.000 0.120 3 120113774 intron variant C/A snv 0.74 1
rs7638459
TRPC1
1.000 0.120 3 142771309 intron variant T/C snv 0.35 1
rs7639705
MCF2L2
1.000 0.120 3 183309754 missense variant T/G snv 0.26 0.27 1
rs953239
TRPC1
1.000 0.120 3 142727363 intron variant A/C snv 0.46 1
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs11538209
ALB
1.000 0.120 4 73404356 missense variant T/C snv 2
rs58624704
ALB
0.925 0.200 4 73410325 missense variant G/A snv 8.0E-06 3.5E-05 2
rs10019835
GUCY1A1
1.000 0.120 4 155712034 intron variant T/A;C snv 1
rs140407862
WFS1
1.000 0.120 4 6301015 missense variant A/G snv 4.4E-05 1.0E-04 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17