Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs2073617
COLEC10 ; TNFRSF11B
0.776 0.360 8 118952044 upstream gene variant G/A snv 0.58 9
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 9
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 7
rs1864325
MAPT
0.882 0.160 17 45900461 intron variant C/T snv 0.14 6
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs3130340
TSBP1-AS1
0.851 0.200 6 32276850 intron variant T/C snv 0.25 5
rs4355801 0.882 0.120 8 118911634 regulatory region variant A/G;T snv 5
rs7524102 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 5
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 5
rs9921222
AXIN1
0.925 0.120 16 325782 intron variant C/T snv 0.51 5
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58 4
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 4
rs2414095
CYP19A1 ; MIR4713HG
15 51232095 intron variant A/G snv 0.69 4
rs3018362 0.882 0.120 18 62414860 upstream gene variant A/G snv 0.67 4
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs6959212 7 38088724 intergenic variant T/C;G snv 4
rs72699866
RIN3
14 92648442 intron variant G/A snv 0.14 4
rs7521902
LOC105376850
1.000 0.040 1 22164231 intergenic variant C/A snv 0.22 4
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 4
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 4
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv 3
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 3
rs10085588
LOC105375412 ; SEM1 ; LOC105375411
1.000 0.080 7 96508362 intron variant A/G snv 0.72 3
rs1107748
LINC02594
1.000 0.080 17 43696446 intron variant T/C snv 0.54 3