Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
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
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs754688962 0.851 0.200 2 197402637 missense variant T/C;G snv 5
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs1057519956 0.827 0.200 2 218583025 missense variant T/C snv 5
rs1057519957 0.827 0.200 2 218583026 missense variant C/G snv 5
rs34968276 0.776 0.240 9 21971110 stop gained G/A;C;T snv 9
rs1057519881 0.776 0.240 9 21971111 missense variant T/C snv 8
rs121913385 0.763 0.240 9 21971112 missense variant G/A;C snv 8
rs770248150 0.807 0.240 12 25225713 missense variant T/A;G snv 4.0E-06 6
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs1057519884 0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs398124146 0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs28931588 0.701 0.200 3 41224606 missense variant G/A;C;T snv 14
rs121913396 0.732 0.200 3 41224607 missense variant A/C;G;T snv 11
rs1057519886 0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs121913399 0.724 0.200 3 41224612 missense variant G/A;C snv 10