Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1049253
CASP3
0.851 0.160 4 184627797 3 prime UTR variant A/G snv 0.13 4
rs763015080
EDNRA
0.851 0.120 4 147539821 missense variant G/A snv 4.1E-06 4
rs971074
ADH7
0.925 0.040 4 99420704 synonymous variant C/T snv 0.12 0.13 3
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs6898743
GHR
0.776 0.160 5 42602390 intron variant C/G snv 0.78 9
rs749710704
BHMT ; DMGDH
0.790 0.160 5 79119289 missense variant C/G;T snv 4.0E-06; 4.0E-06 7
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs4946936
FOXO3
0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv 8
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs11752942
LINC00951 ; TDRG1
0.882 0.080 6 40354019 intron variant A/G snv 0.46 3
rs752153816
VEGFA
0.882 0.120 6 43780848 missense variant G/A;C snv 4.0E-06; 4.0E-06; 1.2E-05; 3.6E-05 3
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs3218536
XRCC2
0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs747126003
IL6-AS1 ; IL6
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs2285947
DNAH11
0.807 0.120 7 21544470 intron variant G/A snv 0.44 7
rs3218373
XRCC2
0.827 0.120 7 152677078 upstream gene variant C/A snv 0.15 5
rs10950641
SNX8
0.925 0.040 7 2294751 intron variant G/A snv 2.9E-02 4