Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs879254933
MIR6886 ; LDLR
0.882 0.160 19 11113708 frameshift variant -/A delins 4
rs906600204
LLGL2
1.000 0.080 17 75569087 frameshift variant -/ACTT delins 1
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs1555808111
LDLR
0.925 0.160 19 11123284 frameshift variant -/GCTG delins 3
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs34234989
MMP24-AS1-EDEM2 ; PROCR
0.882 0.120 20 35186731 intron variant A/- delins 0.40 5
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs7248488
ZNF208
0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs1524668
ADAM17
0.851 0.160 2 9557243 upstream gene variant A/C snv 0.64 4
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 3
rs1711972
FOXF2 ; LOC105374880
0.925 0.160 6 1388953 upstream gene variant A/C snv 4.7E-02 3
rs3818416
EDNRB-AS1 ; EDNRB
1.000 0.080 13 77900333 intron variant A/C snv 0.75 3
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 3
rs17110453
CYP2C8
0.925 0.080 10 95069772 upstream gene variant A/C snv 0.11 2
rs3093105
CYP4F2
0.925 0.080 19 15897578 missense variant A/C snv 0.16 0.18 2
rs6690733
DOCK7
1.000 0.080 1 62594640 intron variant A/C snv 0.43 2
rs783396
CRYBG1
1.000 0.080 6 106539495 missense variant A/C snv 0.93 0.93 2
rs11498973 1.000 0.080 10 84732025 intergenic variant A/C snv 0.19 1
rs2230501
PRKCH
1.000 0.080 14 61457523 synonymous variant A/C snv 3.1E-02 1.6E-02 1
rs6577555
MIR34AHG ; MIR34A
1.000 0.080 1 9152228 intron variant A/C snv 0.74 1
rs7202008
ZDHHC7
1.000 0.080 16 84985897 intron variant A/C snv 1.2E-02 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15