Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10030601
IQCM
1.000 0.040 4 149804060 intron variant T/C snv 0.22 1
rs10157763
AKT3
1.000 0.040 1 243831739 intron variant T/A;C snv 2
rs10234411
ABCB1
1.000 0.040 7 87535576 intron variant T/A;C;G snv 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs104894358
KCNA1
0.882 0.120 12 4912627 stop gained C/G;T snv 4.0E-06 3
rs10496964 0.925 0.040 2 144602342 intergenic variant C/T snv 0.12 2
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1057516064
ND3 ; COX3 ; ATP6 ; ND4L ; ND4
0.925 0.120 MT 9237 missense variant G/A snv 3
rs1057516085
KCNQ2
0.827 0.080 20 63444747 missense variant C/T snv 8
rs1057518801
SCN3A
0.851 0.080 2 165130238 missense variant A/G snv 5
rs1057518988
GRIN2B
0.925 0.040 12 13571859 missense variant T/C snv 3
rs1057520918
CACNA1A
0.790 0.160 19 13262780 missense variant C/T snv 11
rs1057910
CYP2C9
0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 12
rs1064797102
OTUD6B-AS1 ; OTUD6B
0.827 0.120 8 91071136 splice acceptor variant A/G snv 15
rs1064797103
OTUD6B
0.827 0.280 8 91078597 missense variant A/G snv 9
rs10818488
C5-OT1
0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 8
rs10868235
NTRK2
0.925 0.040 9 84878840 intron variant C/T snv 0.40 6
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 11
rs1109771
NOTCH4
1.000 0.040 6 32219828 intron variant A/G snv 0.57 0.54 1
rs111577701 1.000 0.040 3 168143620 intergenic variant C/T snv 0.13 1
rs111908689 1.000 0.040 11 85938055 downstream gene variant C/G;T snv 1
rs11214136
BCO2
1.000 0.040 11 112211286 intron variant T/C snv 0.12 1
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64