Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs2737190 0.827 0.120 9 117701903 upstream gene variant G/A snv 0.52 6
rs7762544 0.882 0.040 6 41411577 intergenic variant G/A snv 0.81 3
rs1595009 1.000 0.040 4 73968939 intergenic variant C/T snv 0.61 1
rs3826782
ADGRE1
0.882 0.040 19 6887725 intron variant G/A snv 8.6E-02 3
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1342913
BRINP3
0.851 0.040 1 190151895 intron variant G/A snv 0.61 4
rs113420705
CASP3 ; PRIMPOL
0.925 0.160 4 184649399 5 prime UTR variant T/C snv 0.31 4
rs4647602
CASP3 ; PRIMPOL
0.925 0.120 4 184648647 intron variant G/T snv 9.5E-02 4
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1058885
CSF1
0.925 0.080 1 109923844 missense variant T/C snv 0.38 0.39 2
rs2297706
CSF1
1.000 0.040 1 109914244 intron variant C/A;T snv 0.22 0.25 1
rs333967
CSF1
1.000 0.040 1 109917151 intron variant C/T snv 0.28 1
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1800972
DEFB1
0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 16
rs11362
DEFB1
0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1050501
FCGR2B
0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs396991
FCGR3A
0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53