Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886039814 0.807 0.200 4 39218060 missense variant C/G snv 13
rs754279998 0.776 0.360 17 58208153 inframe deletion GAG/- delins 2.0E-05 1.4E-05 10
rs886039795 0.851 0.160 17 7403143 frameshift variant CACTCAGAGCCTGGTAGTAAAA/- del 10
rs201037487 0.925 0.120 19 38407003 stop gained C/G;T snv 4.0E-06; 1.4E-04; 4.0E-06 4.9E-05 7
rs118203918 0.882 0.160 6 53016099 missense variant C/T snv 4.0E-06 6
rs786205567 0.925 0.120 3 129500070 splice donor variant T/C snv 5
rs1057519335 0.925 0.040 9 35792968 missense variant T/A snv 5
rs786201032 0.925 0.120 11 299372 missense variant G/A snv 4
rs1057518817 1.000 0.080 9 35805944 frameshift variant GTGGTCCTTTC/- del 4
rs757744435 1.000 0.080 9 35794009 missense variant A/G;T snv 4