Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657152 0.821 0.214 None NA snp 0.41 15
rs687289 0.923 0.143 None NA snp 0.39 9
rs507666 0.846 0.036 None NA snp 0.17 4
rs77641731
ABO
1.000 0.036 9 133257521 missense variant snp 3
rs1588635 1.000 0.071 9 97775520 intergenic variant A/C snp 0.71 2
rs11974269 7 21108059 intergenic variant A/C snp 0.16 1
rs1366046 3 42867283 3 prime UTR variant A/C snp 0.35 1
rs16933006 9 15335916 intergenic variant A/C snp 0.14 1
rs433755 5 9474834 intron variant A/C snp 0.51 1
rs4362633 20 17464490 non coding transcript exon variant A/C snp 0.10 1
rs7027030 9 97788173 intergenic variant A/C snp 0.72 1
rs7179495 15 32608094 intron variant A/C snp 0.78 1
rs7998314 13 93580876 intron variant A/C snp 0.76 1
rs920016 8 68628983 intron variant A/C snp 0.14 1
rs7652290 3 46258274 intron variant A/C,G snp 3.2E-05; 0.37 1
rs765684 2 75232542 intergenic variant A/C,G snp 5.4E-03 1
rs10983761 9 97791675 intergenic variant A/C,G,T snp 0.72; 3.2E-05 1
rs2449215 8 3630816 intron variant A/C,G,T snp 0.36 1
rs1443512 12 53948900 regulatory region variant A/C,T snp 0.67 1
rs2228468 1.000 0.071 3 42865620 missense variant A/C,T snp 0.43; 8.3E-03 0.35; 7.4E-03 1
rs316662 1 84321629 intron variant A/C,T snp 0.88; 1.6E-04 1
rs2075650 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 16
rs9930506
FTO
1.000 0.071 16 53796553 intron variant A/G snp 0.36 5
rs10759944 0.923 0.071 9 97794690 intergenic variant A/G snp 0.72 3
rs7850258 0.846 0.179 9 97786731 intergenic variant A/G snp 0.71 3