Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1569175 1.000 0.120 2 200157231 intergenic variant T/C snv 0.88 1
rs6684897 1.000 0.120 1 238128048 intergenic variant C/G snv 0.83 3
rs7896246
ARID5B
0.925 0.120 10 61964631 intron variant A/G snv 0.74 2
rs3942852
PTPRJ
1.000 0.120 11 48093537 intron variant C/T snv 0.69 1
rs4245595
ARID5B
1.000 0.120 10 61963136 intron variant C/T snv 0.69 1
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs8015478
CEBPE
1.000 0.120 14 23116809 downstream gene variant A/C snv 0.68 2
rs4982731 1.000 0.120 14 23116124 downstream gene variant C/T snv 0.68 1
rs7901152
PIP4K2A
1.000 0.120 10 22544224 intron variant G/A snv 0.66 1
rs4982729 1.000 0.120 14 23107402 upstream gene variant T/C snv 0.66 1
rs7073837
ARID5B
0.851 0.120 10 61940136 intron variant A/C snv 0.58 0.64 4
rs4947709
GRB10
1.000 0.120 7 50605210 non coding transcript exon variant T/C snv 0.63 1
rs2191566
ZNF230
0.925 0.200 19 44007237 intron variant G/T snv 0.62 2
rs2036914
F11
0.882 0.160 4 186271327 intron variant T/C snv 0.57 5
rs7075634
PIP4K2A
1.000 0.120 10 22564173 intron variant T/C snv 0.57 1
rs7923074
ARID5B
1.000 0.120 10 61963681 intron variant A/C snv 0.56 1
rs637868
PHGDH
1.000 0.120 1 119714487 splice region variant T/C snv 0.56 3
rs3887825
DDC ; FIGNL1
1.000 0.120 7 50477395 intron variant T/C snv 0.56 2
rs10821938
ARID5B
0.925 0.120 10 61965014 intron variant A/C snv 0.56 2
rs7088318
PIP4K2A
0.851 0.120 10 22564019 intron variant C/A snv 0.55 4
rs11013046
PIP4K2A
1.000 0.120 10 22551654 intron variant C/T snv 0.55 1
rs7803247
DDC ; FIGNL1
1.000 0.120 7 50473045 intron variant T/C snv 0.52 1
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 9