Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs689470
PTGS2
0.776 0.240 1 186671926 3 prime UTR variant G/A;C;T snv 9
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs2229569
SELL ; C1orf112
0.790 0.360 1 169704697 missense variant G/A;T snv 0.21; 3.2E-05 8
rs562556
PCSK9
0.827 0.280 1 55058564 missense variant G/A snv 0.86 0.83 8
rs1194897557
MTHFR
0.827 0.240 1 11796276 missense variant A/G snv 8.0E-06 7
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs12042319
DOCK7
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 6
rs12746200
PLA2G4A
0.851 0.160 1 186880054 intron variant A/G snv 7.3E-02 6
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5
rs71636784
ZDHHC18
1.000 0.040 1 26842709 intron variant T/G snv 0.12 4
rs765625943
MTHFR
0.882 0.200 1 11803417 missense variant G/A snv 4.3E-06 4
rs1361600
MIR12133 ; F3
0.925 0.120 1 94542362 upstream gene variant C/T snv 0.51 3
rs2760061 1 228003374 upstream gene variant T/A snv 0.55 3
rs2774279
USF1 ; ARHGAP30
0.925 0.080 1 161047766 synonymous variant C/T snv 0.27 0.27 3
rs3093068 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 3
rs35479618
MIR8083 ; NPR1
1 153689947 missense variant G/A snv 9.5E-03 1.1E-02 3
rs8179183
LEPR
1.000 0.080 1 65610269 missense variant G/C;T snv 3
rs1560833 1 153362049 downstream gene variant G/A snv 0.22 2
rs16857031
NOS1AP ; LOC105371475
1 162143120 intron variant C/G snv 0.18 2
rs2493296
PRDM16
1 3410468 intron variant C/G;T snv 2
rs2613498
LOC105378797
1 72287256 intron variant C/T snv 0.20 2
rs4350231
DOCK7
1 62456989 intron variant G/A snv 0.33 2
rs6684311 1.000 0.120 1 166516654 intergenic variant C/G snv 0.22 2
rs6686889 1 24703979 upstream gene variant C/A;G;T snv 2