Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs730880850 0.923 0.036 14 23431584 splice donor variant C/T snp 4.0E-06 3
rs267607003 0.923 0.036 10 110812310 missense variant C/A,G,T snp 3
rs267607004 0.923 0.036 10 110812304 missense variant G/A snp 3
rs104894655 0.923 0.143 17 39665762 stop gained C/T snp 3
rs74315380 0.878 0.071 1 201364366 missense variant G/A,C snp 3
rs373040154 0.923 0.143 2 178617388 stop gained G/A,T snp 3.2E-05 3
rs397517643 0.923 0.143 2 178592914 frameshift variant AC/A in-del 3
rs397517689 0.923 0.036 2 178574530 stop gained G/A snp 4.0E-06 3
rs397517735 0.923 0.143 2 178559309 splice donor variant A/T snp 4.4E-06 3.2E-05 3
rs557312035 0.923 0.143 2 178564811 stop gained G/A,C,T snp 8.1E-06 3
rs727503586 0.923 0.143 2 178589508 stop gained A/T snp 3
rs727505284 0.923 0.143 2 178565416 stop gained G/A snp 8.0E-06 3
rs770038577 0.923 0.143 2 178561042 stop gained G/A,T snp 4.0E-06 3.2E-05 3
rs869025545 0.923 0.143 2 178566448 stop gained G/A snp 3
rs397517065 15 34792471 missense variant G/A snp 2
rs397516881 1.000 10 119676917 missense variant G/A snp 2
rs727505109 1.000 10 119676621 frameshift variant CC/C in-del 2
rs111033559 0.923 0.036 6 118558946 missense variant C/T snp 2
rs62636495
DES
0.923 0.179 2 219418500 missense variant C/T snp 2
rs397516973
DSP
1.000 0.071 6 7565448 stop gained C/A,T snp 1.2E-05 2
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