Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918393
APOE
0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs28362286
PCSK9
0.851 0.080 1 55063542 stop gained C/A;T snv 5.6E-04 6
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs5743611
TLR1
0.807 0.160 4 38798593 missense variant C/G snv 6.9E-02 7.1E-02 7
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs567170
KL
1.000 0.040 13 33043649 intron variant C/G snv 0.32 1
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs20417
PACERR ; PTGS2
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs4606
RGS2
0.752 0.120 1 192812042 3 prime UTR variant C/G;T snv 16
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs267606661
APOE
0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs67608943
PCSK9
0.851 0.080 1 55046549 stop gained C/G;T snv 1.9E-04 8
rs1764391
SMIM12 ; GJA4 ; LOC105378642
0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs33932899
LOC105371082 ; RMI2 ; SOCS1
0.851 0.240 16 11254354 intron variant C/G;T snv 4