Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12573787 1.000 0.080 10 87863959 5 prime UTR variant G/A;C snv 1
rs1343187782 1.000 0.080 3 37298923 missense variant T/C snv 4.0E-06 1
rs1414109649 1.000 0.080 5 40765164 missense variant A/G snv 4.0E-06 1
rs1487152821 1.000 0.080 6 33180274 missense variant G/A snv 7.0E-06 1
rs281860566 1.000 0.080 6 31270339 missense variant C/T snv 1
rs34549764 1.000 0.080 9 130862953 missense variant A/G snv 2.6E-03 2.5E-03 1
rs369488601 1.000 0.080 22 23181175 missense variant G/A;C snv 1.9E-05; 9.7E-05 1
rs375912312 1.000 0.080 1 22588916 missense variant C/T snv 7.0E-06 1
rs4795519 1.000 0.080 17 27214252 intergenic variant A/C snv 0.43 1
rs532354124 1.000 0.080 1 197103274 missense variant T/C;G snv 1
rs6931104 1.000 0.080 6 151465042 intron variant G/A snv 0.54 1
rs754541813 1.000 0.080 3 58123401 synonymous variant C/T snv 6.8E-05 2.8E-05 1
rs754736070 1.000 0.080 4 99597206 missense variant T/C snv 8.0E-06 7.0E-06 1
rs755796482 1.000 0.080 12 111447512 missense variant G/A snv 4.1E-06 8.1E-06 1
rs760454379 1.000 0.080 7 50400082 missense variant G/A snv 1.6E-05 7.0E-06 1
rs766124888
BCR
1.000 0.080 22 23253817 missense variant C/A;G snv 4.0E-06; 4.0E-06 1
rs768288452 1.000 0.080 22 23181822 missense variant A/G snv 4.1E-06 1
rs775014154 1.000 0.080 22 23181637 missense variant C/T snv 5.8E-05 7.0E-05 1
rs886063722 1.000 0.080 9 136677118 missense variant G/A snv 4.0E-06 1
rs9610915 1.000 0.080 22 38215073 3 prime UTR variant C/G snv 0.48 0.41 1
rs121908587 0.827 0.120 4 54278380 missense variant C/T snv 6
rs387906517 0.827 0.120 9 130862919 missense variant G/A snv 6
rs121913448 0.827 0.120 9 130862976 missense variant G/A snv 5
rs121913461 0.851 0.120 9 130862970 missense variant T/C snv 5
rs1060500091 0.882 0.120 3 128481887 missense variant A/C snv 4