Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7790522 1.000 0.120 7 7242918 intron variant A/G snv 0.30 1
rs3796283
LPP
0.851 0.200 3 188885163 3 prime UTR variant A/G;T snv 4
rs11084377 1.000 0.120 19 54875434 intron variant A/G;T snv 1
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs11264793 1.000 0.120 1 157677736 3 prime UTR variant A/T snv 0.28 1
rs11089788 0.851 0.120 22 36355056 intron variant C/A snv 0.46 5
rs11264794 1.000 0.120 1 157677999 3 prime UTR variant C/A snv 0.63 2
rs12022418 1.000 0.120 1 192565977 intron variant C/A snv 0.64 1
rs1362970 1.000 0.120 12 95658750 3 prime UTR variant C/A snv 0.47 1
rs2523946 0.925 0.200 6 29974166 upstream gene variant C/A;G;T snv 2
rs4077515 0.763 0.360 9 136372044 missense variant C/A;T snv 4.0E-06; 0.41 11
rs2364480 0.925 0.120 12 6386109 synonymous variant C/A;T snv 0.77; 2.0E-05 2
rs3129269 1.000 0.120 6 33129837 downstream gene variant C/A;T snv 1
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2195239 0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28 7
rs9314614 1.000 0.120 8 6840209 intron variant C/G snv 0.61 2
rs77370625 1.000 0.120 19 57328138 missense variant C/G snv 5.8E-03 2.8E-03 1
rs887280103
ACE
1.000 0.120 17 63477294 missense variant C/G snv 1.4E-05 1
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1126616 0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26 8
rs2378456
LPP
0.807 0.200 3 188885218 3 prime UTR variant C/G;T snv 6
rs3204008 1.000 0.120 14 51968341 3 prime UTR variant C/G;T snv 1
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21