Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs148704956
IL17A
0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs536562413
FBXO11 ; MSH6
0.732 0.240 2 47799934 missense variant A/G snv 1.2E-05 7.0E-06 15
rs750521832
MMP8
0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 11
rs6022999
CYP24A1
0.790 0.160 20 54171474 intron variant A/G snv 0.36 9
rs2236338
GZMB
0.851 0.120 14 24631076 missense variant A/G snv 0.24 0.25 6
rs1902432
PCAT1 ; LOC105375751
0.851 0.120 8 127012566 intron variant A/G snv 0.25 4
rs2770150 0.925 0.080 9 117700861 upstream gene variant A/G snv 0.22 4
rs7987649
FLT1
0.925 0.080 13 28320278 intron variant A/G snv 0.35 4