Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111033199 0.878 0.179 7 107672245 missense variant G/A,C,T snp 1.8E-04; 4.0E-06 6.4E-05 4
rs539699299 0.846 0.143 7 107661725 missense variant C/A,G snp 3.2E-05 4
rs111033220 0.923 0.143 7 107690203 missense variant C/G,T snp 4.0E-06; 1.8E-04 6.4E-05 3
rs111033256 0.923 0.143 7 107675060 missense variant T/A snp 2.0E-04 3
rs111033303 0.923 0.143 7 107674970 missense variant G/T snp 3.0E-04 2.9E-04 3
rs111033305 0.923 0.143 7 107690200 missense variant G/A,C snp 1.0E-04; 8.0E-06 6.4E-05 3
rs111033307 0.923 0.143 7 107694473 missense variant T/G snp 1.0E-04 9.6E-05 3
rs111033308 0.923 0.143 7 107695984 missense variant G/A snp 2.0E-05 6.4E-05 3
rs111033318 0.923 0.143 7 107702050 missense variant T/A snp 3
rs121908361 0.923 0.143 7 107689156 missense variant A/G snp 3
rs121908362 0.923 0.143 7 107710132 missense variant A/G snp 1.2E-04 6.4E-05 3
rs121908363 0.923 0.143 7 107710126 missense variant C/T snp 5.2E-05 3
rs121908364 0.923 0.143 7 107689166 missense variant C/T snp 3
rs145254330 0.923 0.143 7 107672182 missense variant C/T snp 3.3E-04 3.2E-05 3
rs201562855 0.923 0.143 7 107690148 missense variant A/T snp 4.0E-06 3
rs28939086 0.923 0.143 7 107690220 missense variant A/C,G snp 2.0E-04; 4.0E-06 1.3E-04 3
rs542620119 0.923 0.143 7 107674302 missense variant G/C snp 9.1E-05 3.2E-05 3
rs763006761 0.923 0.143 7 107700135 missense variant A/G snp 1.6E-05 3
rs80338848 0.923 0.143 7 107675051 missense variant T/C snp 2.7E-04 4.5E-04 3
rs111033205 0.923 0.214 7 107661726 stop gained G/C,T snp 9.3E-05; 6.2E-06 2.2E-04 3
rs1057517303 1.000 0.143 7 107710192 stop gained T/A,C snp 3.2E-05 2
rs111033212 0.923 0.143 7 107689054 missense variant T/A,C snp 4.0E-06; 8.6E-04 4.5E-04 2
rs111033244 1.000 0.143 7 107690125 missense variant A/G snp 1.1E-04 9.6E-05 2
rs111033245 1.000 0.143 7 107683355 splice donor variant G/T snp 2
rs111033254 1.000 0.143 7 107698085 missense variant T/C snp 2.0E-05 2