Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11207010 1.000 0.080 1 57337214 intron variant G/C snv 0.41 1
rs12061812 1.000 0.080 1 57336931 intron variant C/A snv 0.30 1
rs12087888 1.000 0.080 1 57337087 intron variant T/C snv 0.41 1
rs1252688154 1.000 0.080 1 155187520 missense variant C/T snv 4.0E-06 1
rs12728900 1.000 0.080 1 26420316 intron variant G/A snv 0.29 1
rs1414493 1.000 0.080 1 241523216 upstream gene variant A/G snv 0.62 1
rs17425189 1.000 0.080 1 57397277 intron variant T/C snv 0.12 1
rs228727 1.000 0.080 1 7787776 non coding transcript exon variant T/A;C snv 1
rs267650 1.000 0.080 1 57330108 intron variant T/C snv 0.36 1
rs3176447 1.000 0.080 1 50968015 5 prime UTR variant T/A snv 7.7E-02 1
rs375294990 1.000 0.080 1 155192150 missense variant G/C snv 8.0E-06 5.6E-05 1
rs3768160
MTR
1.000 0.080 1 236899132 3 prime UTR variant T/C snv 6.4E-02 1
rs3909556 1.000 0.080 1 57381313 intron variant C/A;T snv 1
rs652625 1.000 0.080 1 12165294 upstream gene variant T/A snv 0.14 1
rs6587361 1.000 0.080 1 229883301 intron variant G/A snv 0.22 1
rs7525160
CR1
1.000 0.080 1 207495069 upstream gene variant G/C snv 0.29 1
rs784621 1.000 0.080 1 39641113 upstream gene variant T/C snv 0.85 1
rs9660710 1.000 0.080 1 1163962 upstream gene variant A/C;T snv 1
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40