Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 175
rs1799945 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 152
rs738409 0.590 0.536 22 43928847 missense variant C/G snp 0.28 0.22 55
rs12979860 0.608 0.500 19 39248147 intron variant C/T snp 0.38 47
rs5743708 0.605 0.643 4 153705165 missense variant G/A snp 1.7E-02 2.3E-02 45
rs1799864 0.626 0.536 3 46357717 missense variant G/A snp 0.13 0.12 39
rs8099917 0.618 0.464 19 39252525 intergenic variant T/G snp 0.15 38
rs757366142 0.657 0.500 3 46357714 missense variant G/A snp 4.0E-06 27
rs7080536 0.685 0.286 10 113588287 missense variant G/A snp 2.2E-02 2.3E-02 22
rs4950928 0.679 0.464 1 203186754 regulatory region variant G/A,C,T snp 0.75 21
rs1127354 0.685 0.321 20 3213196 missense variant C/A,G snp 7.5E-02 7.0E-02 21
rs763059810 0.707 0.464 2 136115750 missense variant T/C snp 4.0E-06 20
rs58542926 0.707 0.250 19 19268740 missense variant C/T snp 6.5E-02 5.8E-02 20
rs9275572 0.685 0.321 6 32711222 intergenic variant A/G,T snp 0.57; 3.2E-05 17
rs2287622 0.707 0.179 2 168973818 missense variant A/C,G,T snp 0.57 0.57 16
rs4444903
EGF
0.707 0.179 4 109912954 5 prime UTR variant A/G snp 0.50 16
rs10741657 0.715 0.286 11 14893332 intergenic variant A/G snp 0.64 15
rs3077 0.734 0.321 6 33065245 3 prime UTR variant A/G snp 0.28 12
rs2569190 0.724 0.286 5 140633331 5 prime UTR variant A/G snp 0.58 12
rs12980275 0.769 0.143 19 39241143 intergenic variant A/G snp 0.35 11
rs2282679
GC
0.744 0.286 4 71742666 intron variant T/G snp 0.22 11
rs153109 0.744 0.357 16 28507775 intron variant T/C snp 0.45 11
rs2596542 0.756 0.143 6 31398818 intergenic variant C/T snp 0.38 10
rs368234815 0.769 0.143 19 39248514 frameshift variant CTT/C,CG in-del 9
rs12785878 0.784 0.393 11 71456403 intron variant G/A,T snp 3.2E-05; 0.55 9