Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 8
rs34670419
ZKSCAN5
1.000 0.080 7 99533211 3 prime UTR variant G/A;T snv 7.7E-06; 2.6E-02 7
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 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
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
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 5
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 4
rs6684375 1 22379941 regulatory region variant C/T snv 0.20 4
rs6959212 7 38088724 intergenic variant T/C;G snv 4
rs2414095
CYP19A1 ; MIR4713HG
15 51232095 intron variant A/G snv 0.69 4
rs72699866
RIN3
14 92648442 intron variant G/A snv 0.14 4
rs884205
TNFRSF11A
18 62387624 3 prime UTR variant A/C;T snv 4
rs3130340
TSBP1-AS1
0.851 0.200 6 32276850 intron variant T/C snv 0.25 4
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 3
rs1564981 16 50952397 intergenic variant G/A snv 0.60 3
rs3018362 0.882 0.120 18 62414860 upstream gene variant A/G snv 0.67 3
rs4580892 6 127088737 intron variant C/T snv 0.32 3
rs9525638 13 42554441 regulatory region variant T/C snv 0.37 3
rs9921222
AXIN1
0.925 0.120 16 325782 intron variant C/T snv 0.51 3
rs6929137
CCDC170 ; LOC107986528
0.851 0.160 6 151615542 missense variant G/A snv 0.31 0.36 3
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 3
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 3
rs917727
FAM3C
7 121378525 intron variant C/A;T snv 0.33 3