Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 5
rs713586 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 5
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4
rs12714415 2 651430 intergenic variant T/C snv 0.19 4
rs939583 1.000 0.080 2 622531 intergenic variant C/T snv 0.85 4
rs13013484 2 27765954 intergenic variant G/A snv 0.61 3
rs13396935 2 653195 intergenic variant G/A snv 0.18 3
rs1561288
EFR3B
2 25146133 3 prime UTR variant C/T snv 0.29 3
rs2867112 2 651349 intergenic variant T/G snv 0.18 3
rs2890652 2 142202362 intergenic variant T/C snv 0.21 3
rs2903492 2 624678 intergenic variant G/A snv 0.85 3
rs4854349 2 647861 intergenic variant T/C snv 0.77 3
rs6545814
ADCY3
2 24908447 intron variant A/G snv 0.53 3
rs7586879
ADCY3
2 24894108 intron variant C/T snv 0.47 3
rs10173167 2 646767 intergenic variant G/A snv 0.82 2
rs10188334 2 653874 regulatory region variant C/A;T snv 0.15 2
rs10193244 2 647580 intergenic variant T/C snv 0.77 2
rs12617233
LINC01122
2 58812863 intron variant T/A;C snv 2
rs12714414 2 651407 intergenic variant T/C snv 0.18 2
rs12999687
DNMT3A
2 25289569 intron variant T/G snv 0.48 2
rs13034723
C2orf88
2 190120954 intron variant G/A snv 0.37 2