Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1020856343 0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06 5
rs10988542 0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs12720356 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 12
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs272893 0.925 0.160 5 132327369 missense variant T/C;G snv 0.58; 4.0E-06 2
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs4869313 0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614