Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs174546 0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs688 0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs1042034 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs174601 0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12