Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8126
TNFAIP2
0.807 0.080 14 103137232 3 prime UTR variant C/T snv 0.63 8
rs10484761 0.807 0.080 6 40834522 intergenic variant T/C snv 0.31 7
rs2285947
DNAH11
0.807 0.120 7 21544470 intron variant G/A snv 0.44 7
rs2014300
RUNX1
0.851 0.080 21 34985564 intron variant A/G;T snv 0.75 5
rs3218373
XRCC2
0.827 0.120 7 152677078 upstream gene variant C/A snv 0.15 5
rs1049253
CASP3
0.851 0.160 4 184627797 3 prime UTR variant A/G snv 0.13 4
rs10950641
SNX8
0.925 0.040 7 2294751 intron variant G/A snv 2.9E-02 4
rs11016879
MGMT
0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
rs1629816
GHRL ; GHRLOS ; SEC13
0.851 0.080 3 10294607 non coding transcript exon variant G/A;C snv 4
rs4775319
RORA
0.925 0.040 15 60921365 intron variant G/A snv 0.62 4
rs4855883
APEH
0.851 0.080 3 49673881 upstream gene variant G/A;C snv 4
rs6796803 0.925 0.040 3 186746318 intron variant T/A;C snv 4
rs985325188
APEX1 ; OSGEP
0.851 0.080 14 20456806 missense variant A/C snv 4
rs10882272
FFAR4
0.925 0.040 10 93588425 3 prime UTR variant T/C snv 0.44 3
rs11752942
LINC00951 ; TDRG1
0.882 0.080 6 40354019 intron variant A/G snv 0.46 3
rs1667255 0.925 0.040 18 31607316 intergenic variant A/C;G;T snv 3
rs876659477
TP53
0.882 0.040 17 7673730 missense variant T/C snv 3
rs1183646267
ATM
0.925 0.040 11 108281026 missense variant A/G snv 2
rs16943176
RAD51C ; TEX14
0.925 0.040 17 58692526 upstream gene variant G/A;C snv 2
rs17222691
TEX14 ; RAD51C
0.925 0.040 17 58693735 3 prime UTR variant C/T snv 0.17 2
rs3782116
SIRT3
0.925 0.040 11 223119 3 prime UTR variant T/C snv 0.74 2
rs4150403
ERCC3
0.925 0.040 2 127292492 3 prime UTR variant C/T snv 5.7E-02 2
rs522962
PTGIS
0.925 0.040 20 49526825 intron variant T/C snv 0.61 2
rs554194414
KIDINS220
0.925 0.040 2 8731250 missense variant T/C snv 2
rs6019902
PTGIS
0.925 0.040 20 49561676 intron variant G/A snv 0.21 2