Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1242982981
CLEC12A
0.851 0.160 12 9984989 missense variant C/T snv 4
rs4148388
ABCC2
1.000 0.160 10 99790008 intron variant G/A;C snv 1
rs2055729 1.000 0.160 8 9935152 intergenic variant G/A snv 0.54 1
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 7
rs17112190
LCOR
1.000 0.160 10 96880089 intron variant G/A snv 0.15 1
rs1423269
ELL2
1.000 0.160 5 95920020 intron variant A/G snv 0.31 1
rs3777189
ELL2
1.000 0.160 5 95917404 intron variant C/G snv 0.34 1
rs56219066
ELL2
0.882 0.160 5 95907227 intron variant T/A;C snv 3
rs3815768
ELL2
1.000 0.160 5 95900755 missense variant C/T snv 0.27 0.29 1
rs2546191
ELL2
0.851 0.160 5 95896837 intron variant G/A snv 0.38 4
rs1934951
CYP2C8
0.925 0.160 10 95038791 intron variant C/T snv 0.24 4
rs1428
MIR17HG
0.882 0.200 13 91354516 non coding transcript exon variant C/A;T snv 3
rs7336610
MIR17HG
0.827 0.240 13 91352883 intron variant C/T snv 0.47 5
rs4284505
MIR19A ; MIR17 ; MIR17HG ; MIR20A ; MIR18A ; MIR19B1
1.000 0.160 13 91349218 non coding transcript exon variant A/G snv 0.51 1
rs267606870
IDH2
0.763 0.280 15 90088703 missense variant G/A;C snv 11
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs2231137
ABCG2
0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 13
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs4240803
SLC7A5 ; LOC107987237
0.851 0.240 16 87855597 intron variant G/A;C;T snv 4
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 12
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs201478192
KIDINS220
0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 12
rs4240807 0.851 0.160 16 85951755 downstream gene variant A/C snv 0.76 4