Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs397516436 0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs138729528 0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs1057519045 0.851 0.160 10 121498522 missense variant T/G snv 6
rs1057519854 0.882 0.080 10 121488063 missense variant A/T snv 5
rs1057519901 0.925 0.080 10 121498525 missense variant T/G snv 5
rs121913476 0.851 0.080 10 121498520 missense variant A/C;T snv 5