Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12517906 5 180743819 upstream gene variant C/A;T snv 0.11 1
rs12705992 7 114789947 regulatory region variant G/A snv 0.72 1
rs13029479 2 655222 regulatory region variant G/A snv 0.13 1
rs151204774 11 21580341 downstream gene variant AATT/- delins 7.4E-02 1
rs182624399 11 70019090 intron variant C/T snv 8.9E-03 1
rs1840440 18 25677222 intergenic variant T/C;G snv 1
rs1973993 1 96478438 intergenic variant T/C snv 0.49 1
rs630372 1 177916627 intron variant G/A;T snv 1
rs6440919 3 153982187 upstream gene variant C/T snv 0.47 1
rs6735049 2 630569 intergenic variant T/A;C snv 1
rs6780892 3 7947364 downstream gene variant G/A;T snv 1
rs72989246 18 60053966 TF binding site variant C/T snv 8.1E-02 1
rs73144267 7 76923428 downstream gene variant T/C snv 0.23 1
rs7336332 13 27484267 upstream gene variant A/G snv 0.19 1
rs80116344 18 60281167 intergenic variant G/A snv 3.9E-02 1
rs9313296 5 165950694 intergenic variant G/C snv 0.13 1
rs965178 18 25681256 intergenic variant T/C snv 0.53 1
rs16877106
ANAPC4
4 25401644 intron variant C/T snv 4.9E-02 1
rs112037309
ARHGEF38 ; INTS12
4 105695979 intron variant G/A snv 6.7E-02 1
rs6416056
BDNF-AS ; LINC00678
11 27625198 intron variant G/A snv 0.71 1
rs534356339
CCSER1
4 91335712 intron variant GAT/- del 3.4E-03 1
rs286028
DLG2
11 85394069 intron variant A/C;T snv 1
rs4145878
H3C4 ; H2BC7
6 26197818 intron variant T/A snv 0.58 1
rs765876
HIVEP2
6 142864754 intron variant A/G snv 0.43 1
rs7948458
IGF2 ; INS-IGF2
11 2151600 intron variant A/C snv 0.76 1