Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2250889
SLC12A5-AS1 ; MMP9
0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs2970847
PPARGC1A
0.882 0.200 4 23814301 synonymous variant T/C snv 0.84 0.86 3
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs2682818
MIR618 ; LOC105369869 ; LIN7A
0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs790056
F11R
0.925 0.080 1 160999795 intron variant C/T snv 0.81 0.83 2
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14
rs9912300
ACLY
0.827 0.120 17 41869011 intron variant G/A;C;T snv 4.2E-06; 0.78 5
rs590352
ATXN7L3B
1.000 0.080 12 74538379 synonymous variant G/C snv 0.77 0.64 1
rs2243518
CDH17
1.000 0.080 8 94176622 stop gained T/A;C snv 0.77 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70 9
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1982151
RMI1
0.807 0.120 9 84002350 missense variant A/G;T snv 0.73 9
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs462779
MFSD4B ; REV3L
0.851 0.120 6 111374684 missense variant G/A snv 0.72 0.67 4
rs361863
ISX
1.000 0.080 22 35067169 missense variant A/G snv 0.71 0.73 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs1444601
TOPBP1
1.000 0.080 3 133611099 synonymous variant G/A snv 0.69 0.72 1
rs373572
RAD18
0.882 0.120 3 8913705 missense variant C/T snv 0.68 0.70 6
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs12303082
FAM186A
1.000 0.080 12 50360780 missense variant T/G snv 0.67 0.64 1