Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs3099844 0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 13
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40