Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4382936
P2RY2
1.000 0.120 11 73241355 non coding transcript exon variant A/C snv 0.36 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs3754701
RAMP1
0.882 0.120 2 237858561 upstream gene variant A/C;T snv 4
rs2238634
TBXA2R
0.925 0.200 19 3604731 intron variant A/C;T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs2227631
SERPINE1
0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs147377392
THBD
0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs4523
TBXA2R
0.776 0.280 19 3595796 missense variant A/G snv 0.56 0.66 8
rs1537378
CDKN2B-AS1
0.882 0.160 9 22061615 intron variant A/G snv 0.73 4
rs12659
SLC19A1
0.925 0.120 21 45531642 synonymous variant A/G snv 0.58 0.57 2
rs2278986
SCARB1
0.925 0.120 12 124814823 intron variant A/G snv 0.28 2
rs710968
LIMK1
0.925 0.120 7 74083398 intron variant A/G snv 0.75 2
rs750272074
ROS1
1.000 0.120 6 117362705 synonymous variant A/G snv 4.0E-06 2
rs1207570776
DNAJC10
1.000 0.120 2 182757711 missense variant A/G snv 1
rs2275235
CTSS
1.000 0.120 1 150757803 intron variant A/G snv 0.34 1
rs9621187
SMTN
1.000 0.120 22 31103532 non coding transcript exon variant A/G snv 0.35 1