Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 8
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 8
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs11694173
THADA
0.827 0.080 2 43363760 intron variant G/A snv 0.14 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs3110697
IGFBP3
0.827 0.160 7 45915430 intron variant A/G snv 0.58 7
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 7
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs13101828
DGKQ
0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs2067087
HOTTIP ; HOXA13
1.000 0.080 7 27202041 non coding transcript exon variant G/C;T snv 6
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62 6
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6