Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs4775319
RORA
0.925 0.040 15 60921365 intron variant G/A snv 0.62 4
rs6796803 0.925 0.040 3 186746318 intron variant T/A;C snv 4
rs762384959
OSGEP ; APEX1
0.925 0.040 14 20456680 missense variant G/C snv 8.0E-06 4
rs10882272
FFAR4
0.925 0.040 10 93588425 3 prime UTR variant T/C snv 0.44 3
rs1667255 0.925 0.040 18 31607316 intergenic variant A/C;G;T snv 3
rs4804217
PCP2
1.000 0.040 19 7634461 intron variant C/T snv 0.29 3
rs876659477
TP53
0.882 0.040 17 7673730 missense variant T/C snv 3
rs971074
ADH7
0.925 0.040 4 99420704 synonymous variant C/T snv 0.12 0.13 3
rs11540483
TAX1BP1
0.925 0.040 7 27787484 missense variant T/A snv 8.2E-02 7.7E-02 2
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
rs4253132
ERCC6
0.925 0.040 10 49493110 splice region variant G/A;T snv 0.89; 4.4E-05 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
rs6125671
PTGIS
0.925 0.040 20 49559061 intron variant C/T snv 0.24 2
rs6598072
SIRT3
0.925 0.040 11 219793 intron variant C/T snv 0.79 2
rs770925903
KIDINS220
0.925 0.040 2 8731740 missense variant C/A;T snv 1.6E-05; 4.0E-06 2
rs7802034
XRCC2
0.925 0.040 7 152655183 intron variant A/C;G snv 2
rs927068
PTGIS
0.925 0.040 20 49561437 intron variant G/T snv 0.32 2