Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs908832
ABCA2
0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96 4
rs121908603
ZFPM2-AS1 ; ZFPM2
0.882 0.120 8 105802189 missense variant A/C;G snv 4.9E-04; 4.0E-06 3
rs2254638
N6AMT1
0.882 0.040 21 28883961 intron variant A/C;G snv 3
rs2383205
CDKN2B-AS1
0.925 0.080 9 22060936 intron variant A/C;G snv 3
rs879254920
LDLR ; MIR6886
0.882 0.120 19 11113665 missense variant A/C;G snv 3
rs2246942
LIPA
0.925 0.040 10 89245129 intron variant A/C;G snv 2
rs1049007
BMP2
1.000 0.040 20 6770387 synonymous variant A/C;G snv 0.67 1
rs12091564 1.000 0.040 1 146039391 upstream gene variant A/C;G snv 1
rs2281027
BTN3A3
1.000 0.040 6 26446477 intron variant A/C;G snv 1
rs656451 1.000 0.040 16 77039597 intergenic variant A/C;G snv 2.4E-03 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs10738609
CDKN2B-AS1
1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs11881940
HNRNPUL1 ; TGFB1
0.925 0.040 19 41302527 non coding transcript exon variant A/C;G;T snv 4.9E-06; 4.9E-06; 0.14 2
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs6505162
NSRP1 ; MIR3184 ; MIR423
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1008438
HSPA1L ; HSPA1A
0.807 0.120 6 31815431 upstream gene variant A/C;T snv 6
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs2298566
SNX19
0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 5