Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs3208008
RTEL1 ; TNFRSF6B ; RTEL1-TNFRSF6B
0.925 0.080 20 63694757 missense variant A/C snv 0.75 0.81 2
rs12155172
LINC01162
0.925 0.080 7 20954872 intron variant A/G snv 0.81 2
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs7017300 1.000 0.080 8 127513023 regulatory region variant C/A snv 0.81 1
rs817826 0.925 0.080 9 107394019 intergenic variant C/T snv 0.81 2
rs4774388
RORA
0.807 0.200 15 61174799 intron variant C/T snv 0.81 6
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs11988857 1.000 0.080 8 127519628 intergenic variant G/A snv 0.80 1
rs1465618
THADA
0.882 0.160 2 43326810 intron variant T/C snv 0.80 3
rs10426628
SULT2B1
0.925 0.080 19 48589173 intron variant A/G snv 0.78 2
rs849141
JAZF1
0.851 0.240 7 28145472 intron variant A/G snv 0.78 6
rs2740574
CYP3A4
0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78 12
rs7662551
LOC107986294 ; LINC00989
0.925 0.080 4 79616484 intron variant G/A snv 0.78 2
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs1369481
NPAS2
0.925 0.080 2 100895497 intron variant T/C snv 0.77 2
rs2758330
SOD2
0.925 0.080 6 159683812 intron variant G/T snv 0.77 2
rs2842958
SOD2
0.925 0.080 6 159687393 intron variant A/G snv 0.77 2
rs45609334
HSD3B1
0.925 0.080 1 119514623 missense variant C/A snv 0.76 2
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs6062509
ZGPAT
0.925 0.080 20 63731211 intron variant G/T snv 0.76 2
rs1570360
VEGFA
0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs3448
GPX1 ; RHOA
0.776 0.240 3 49359318 3 prime UTR variant T/C snv 0.76 8
rs2660
OAS1
0.851 0.160 12 112919637 missense variant G/A snv 0.71 0.75 4
rs2278008
C1QTNF3-AMACR ; AMACR
0.851 0.160 5 33989413 missense variant C/T snv 0.70 0.74 4