Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10106
FPGS
0.851 0.200 9 127813796 3 prime UTR variant T/C snv 0.45 4
rs1020608187
SDS
1.000 0.120 12 113398843 missense variant C/G snv 7.0E-06 1
rs10235796
IKZF1
0.882 0.120 7 50394939 intron variant T/C snv 0.82 3
rs10272724 0.882 0.200 7 50409515 downstream gene variant T/C snv 0.24 4
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs10417924
TGFB1
1.000 0.120 19 41327262 intron variant T/C snv 0.86 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1043618
HSPA1L ; HSPA1A
0.752 0.280 6 31815730 5 prime UTR variant G/A;C;T snv 0.39; 2.0E-05; 4.0E-06 10
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs104893636
HOXD4 ; HOXD3
0.882 0.120 2 176151875 missense variant A/C;T snv 5.2E-06; 7.9E-04 3
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1051296
SLC19A1
0.882 0.120 21 45514947 3 prime UTR variant A/C snv 0.43 0.44 3
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs10519612
IL15
0.882 0.120 4 141732548 intron variant A/C snv 0.10 3
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519743
CRLF2
0.827 0.120 Y 1196852 missense variant A/C snv 6
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs1061581
HSPA1A ; HSPA1L
0.827 0.200 6 31816809 synonymous variant G/A snv 6
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs1076991
MTHFD1
0.925 0.200 14 64388323 5 prime UTR variant T/C;G snv 0.45; 8.1E-06 2
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs10821938
ARID5B
0.925 0.120 10 61965014 intron variant A/C snv 0.56 2
rs10828317
PIP4K2A
0.776 0.280 10 22550699 missense variant T/C snv 9
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7