Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17228212
SMAD3
0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs3829251
NADSYN1
0.851 0.120 11 71483513 intron variant G/A snv 0.21 8
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs4380028
MORF4L1
0.807 0.120 15 78818751 intron variant C/T snv 0.34 7
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs213045
ECE1
0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs2144908
LOC105372629 ; HNF4A
0.851 0.120 20 44357077 intron variant G/A snv 0.18 5
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs4252120
PLG
0.827 0.080 6 160722576 intron variant T/C;G snv 0.21 5
rs7217186
ALOX15
0.827 0.120 17 4636097 intron variant C/T snv 0.45 5
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4
rs2518136
AHSG
0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs33932899
LOC105371082 ; RMI2 ; SOCS1
0.851 0.240 16 11254354 intron variant C/G;T snv 4
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 4
rs4862423
ACSL1
0.882 0.080 4 184805394 intron variant C/T snv 0.37 4
rs7895340
TCF7L2
0.851 0.160 10 113041766 intron variant G/A snv 0.53 4
rs877087
RYR3
0.882 0.080 15 33582074 intron variant T/C;G snv 4
rs212528
ECE1
0.925 0.040 1 21259168 intron variant T/C snv 0.12 3
rs2269422
AGER
0.882 0.040 6 32183517 intron variant T/C snv 1.7E-02 5.8E-03 3
rs4916251
DNM3 ; PIGC
0.882 0.040 1 172377256 intron variant T/A snv 0.70 3