Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11568818 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11902171 0.925 0.080 2 186678500 3 prime UTR variant G/C snv 0.22 6
rs11943456 0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs1197734477 0.925 0.080 10 87961012 missense variant A/G snv 4
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs12338 0.807 0.200 8 11853379 missense variant G/A;C;T snv 8.0E-06; 0.38; 2.4E-05 10
rs12422149 0.827 0.120 11 75172532 missense variant G/A;T snv 0.18 7
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs12757998 0.925 0.080 1 182569343 downstream gene variant C/T snv 0.24 3
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1290923018 0.851 0.160 11 65570699 missense variant G/A snv 4.0E-06 5
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 5
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29