Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs17366743 0.807 0.280 3 186854300 missense variant T/C snv 2.2E-02 2.1E-02 7
rs62625753 0.925 0.120 3 186854237 missense variant G/A snv 3.0E-03 2.9E-03 3
rs199646033 0.925 0.120 3 186854219 stop gained G/A;T snv 4.4E-05; 4.0E-06 3