Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386134243 0.715 0.321 1 156135967 missense variant C/A,T snp 4.0E-06 14
rs74315379 0.821 0.071 1 201364336 missense variant G/A,T snp 1.2E-04 6
rs397516471 0.878 0.071 1 201363348 missense variant C/T snp 4
rs397517889 0.878 0.143 1 156136093 missense variant C/T snp 4
rs45578238 0.878 0.071 1 201361971 inframe deletion ATCT/A in-del 4
rs60682848 0.846 0.143 1 156134838 stop gained C/T snp 4
rs56984562 0.846 0.179 1 156137666 missense variant C/A,G,T snp 3
rs59026483 0.821 0.143 1 156134457 missense variant C/T snp 3
rs61195471 0.846 0.107 1 156134496 missense variant G/A snp 3
rs61444459 0.878 0.143 1 156137667 missense variant G/A,C snp 3
rs74315380 0.878 0.071 1 201364366 missense variant G/A,C snp 3
rs111569862 1.000 0.107 1 156137653 splice acceptor variant G/A,C snp 2
rs267607573 1.000 0.071 1 156134865 stop gained C/T snp 2
rs267607618 1.000 0.071 1 156136350 stop gained C/T snp 2
rs28933091 0.923 0.143 1 156134474 missense variant C/A,G snp 2
rs28933092 1.000 0.036 1 156134497 missense variant A/G,T snp 2
rs28933093 0.923 0.071 1 156130741 missense variant G/A snp 2
rs56816490 0.923 0.107 1 156135913 stop gained G/A,T snp 3.2E-05 2
rs58013325 1.000 0.071 1 156137150 frameshift variant C/CC in-del 2
rs58978449 1.000 0.107 1 156134946 inframe deletion GAAG/G in-del 2
rs59270054 1.000 0.071 1 156115162 missense variant G/A,C snp 2
rs61046466 1.000 0.107 1 156114934 stop gained C/T snp 2
rs727503512 1.000 0.036 1 201363349 missense variant G/A,C,T snp 4.0E-06 2
rs794728589 1.000 0.036 1 156115275 splice donor variant G/A,C snp 2
rs267607554 1 156135925 stop gained C/T snp 1