Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.407 0.786 7 140753336 missense variant snp 4.0E-06 267
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs11540654 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 117
rs1695 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 100
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
rs28934576 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 64
rs1801394 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 60
rs104894230 0.615 0.464 11 534288 missense variant C/A,G,T snp 42
rs121912651 0.618 0.464 17 7674221 missense variant G/A,C snp 4.0E-06 41
rs11540652 0.618 0.464 17 7674220 missense variant C/A,G,T snp 1.2E-05 40
rs104894229 0.634 0.500 11 534289 missense variant C/A,G,T snp 31
rs1056836 0.634 0.500 2 38071060 missense variant G/C snp 0.63 0.50 31
rs121913343 0.638 0.464 17 7673803 missense variant G/A,T snp 1.2E-05 30
rs121913482 0.685 0.393 4 1801837 missense variant C/T snp 30
rs104894228 0.662 0.500 11 534286 missense variant C/A,G,T snp 26
rs121913233 0.657 0.429 11 533874 missense variant T/A,C,G snp 25
rs760043106 0.662 0.357 17 7674947 missense variant A/C,G,T snp 24
rs28934874 0.673 0.429 17 7675161 stop gained G/A,C,T snp 23
rs121912657 0.679 0.464 17 7673806 missense variant C/A,T snp 4.0E-06 22
rs587781525 0.679 0.429 17 7673778 missense variant T/A,C,G snp 22
rs483352697 0.685 0.429 17 7674944 missense variant C/A,G,T snp 4.0E-06 21
rs764146326 0.679 0.429 17 7673779 missense variant C/A,G,T snp 4.0E-06 20
rs863224451 0.692 0.429 17 7673796 stop gained C/A,G,T snp 20
rs104894226 0.692 0.464 11 534285 missense variant C/A,G,T snp 19
rs1057520007 0.699 0.321 17 7674917 missense variant T/A,C,G snp 19