Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs121913238 0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs727503109 0.752 0.320 12 25245277 missense variant T/C snv 17
rs104894360 0.724 0.560 12 25209904 missense variant T/A;C snv 14
rs121913535 0.742 0.320 12 25245348 missense variant C/A;G;T snv 14
rs121913528 0.851 0.160 12 25227349 missense variant C/A;T snv 12
rs104894365 0.827 0.320 12 25245345 missense variant C/T snv 9
rs104894366 0.776 0.400 12 25245284 missense variant G/A;C snv 9
rs121913527 0.807 0.320 12 25225628 missense variant C/A;G;T snv 9
rs770248150 0.807 0.240 12 25225713 missense variant T/A;G snv 4.0E-06 7
rs1057519725 0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06 6
rs104894359 0.851 0.200 12 25227346 missense variant C/G;T snv 5
rs1137282 0.851 0.120 12 25209843 missense variant A/G;T snv 0.19 5
rs12587 0.827 0.200 12 25205894 3 prime UTR variant T/G snv 0.49 5
rs7312175 0.827 0.120 12 25251670 upstream gene variant G/A snv 0.16 5
rs121913236 0.882 0.160 12 25245321 missense variant G/C;T snv 4
rs730880471 0.851 0.280 12 25225709 missense variant C/T snv 4
rs104894361 0.882 0.240 12 25245370 missense variant T/A;C;G snv 4.0E-06 3
rs104894362 0.882 0.200 12 25209894 missense variant G/C snv 3