Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1400094618
MOK
0.882 0.240 14 102229508 missense variant A/G snv 3
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6704078 0.925 0.200 1 216437370 intergenic variant C/T snv 0.94 2
rs759853 0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 6
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs955333 0.882 0.240 6 154626274 intergenic variant A/G snv 0.13 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182