Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607002 1.000 0.036 10 110812303 stop gained C/A,T snp 2
rs267607004 0.923 0.036 10 110812304 missense variant G/A snp 3
rs267607003 0.923 0.036 10 110812310 missense variant C/A,G,T snp 3
rs397516607 1.000 0.036 10 110821356 missense variant G/A snp 2
rs727504859 10 110821365 missense variant G/A snp 1
rs111033559 0.923 0.036 6 118558946 missense variant C/T snp 2
rs397516784 0.923 0.071 6 118558961 inframe deletion AAGA/A in-del 4
rs111033560 0.784 0.071 6 118559037 stop gained T/G snp 1.6E-05 6
rs727502897 10 119651747 frameshift variant CC/C in-del 1
rs727505283 10 119651775 frameshift variant GACCGGCTG/G in-del 1
rs387906875 0.923 0.071 10 119670037 stop gained C/T snp 8.0E-06 3
rs876657634 10 119672477 stop gained C/T snp 1
rs869025365 10 119672657 splice donor variant G/A snp 1
rs869248137 0.923 0.036 10 119676479 stop gained C/T snp 4.0E-06 3
rs727505109 1.000 10 119676621 frameshift variant CC/C in-del 2
rs730880055 10 119676851 stop gained C/T snp 1
rs397516881 1.000 10 119676917 missense variant G/A snp 2
rs63750743 0.923 0.071 3 14141665 missense variant C/T snp 2
rs61046466 1.000 0.107 1 156114934 stop gained C/T snp 2
rs397517895 1 156115072 missense variant C/G snp 1
rs59270054 1.000 0.071 1 156115162 missense variant G/A,C snp 2
rs28933090 0.923 0.143 1 156115172 missense variant T/A,G snp 1
rs267607646 1 156115266 frameshift variant G/GG in-del 1
rs794728589 1.000 0.036 1 156115275 splice donor variant G/A,C snp 2
rs794728597 1 156130627 inframe deletion GAAG/G in-del 1