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
rs2073618
COLEC10 ; TNFRSF11B
0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19
rs3736228
LRP5
0.752 0.400 11 68433827 missense variant C/T snv 0.13 0.11 13
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 9
rs2073617
COLEC10 ; TNFRSF11B
0.776 0.360 8 118952044 upstream gene variant G/A snv 0.58 9
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 7
rs34670419
ZKSCAN5
1.000 0.080 7 99533211 3 prime UTR variant G/A;T snv 7.7E-06; 2.6E-02 7
rs6929137
CCDC170 ; LOC107986528
0.851 0.160 6 151615542 missense variant G/A snv 0.31 0.36 6
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
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
rs9921222
AXIN1
0.925 0.120 16 325782 intron variant C/T snv 0.51 5
rs9303521
LINC02210-CRHR1
0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 5
rs3130340
TSBP1-AS1
0.851 0.200 6 32276850 intron variant T/C snv 0.25 5
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 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
rs1038304
CCDC170 ; LOC107986528
0.882 0.160 6 151612040 intron variant A/G snv 0.58 4
rs2414095
CYP19A1 ; MIR4713HG
15 51232095 intron variant A/G snv 0.69 4
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 4
rs3755955
IDUA
0.925 0.080 4 1000626 missense variant G/A;C snv 0.16; 8.0E-06 4
rs6831280
IDUA
0.925 0.080 4 1002377 missense variant G/A;C snv 0.17 4
rs7521902
LOC105376850
1.000 0.040 1 22164231 intergenic variant C/A snv 0.22 4