Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1927914
TLR4
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14
rs3825172
PSMD9
0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 14
rs74421874
PSMD9
0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs6218
LINC02456 ; HELLPAR ; IGF1
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs3134069
COLEC10 ; TNFRSF11B
0.776 0.320 8 118952749 upstream gene variant A/C snv 9.6E-02 11
rs5742612
LOC105369944 ; IGF1
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs869109213
NOS3
0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins 10
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs12050217
BDKRB1
0.827 0.160 14 96262416 intron variant A/G snv 0.21 6
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs1799768
SERPINE1
0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs3825932
CTSH
0.827 0.360 15 78943104 intron variant T/C snv 0.50 6
rs759853
AKR1B1
0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 6
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv 5
rs551238
EPO
0.925 0.160 7 100723905 downstream gene variant G/T snv 0.62 5