Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1557909821 1.000 0.040 1 151427999 missense variant A/G snv 1
rs1557910728 1.000 0.040 1 151428233 missense variant T/C snv 1
rs1557911386 1.000 0.040 1 151428357 missense variant T/A snv 1
rs1557916296 1.000 0.040 1 151430822 missense variant C/A snv 1
rs1557935477 1.000 0.040 1 151440939 missense variant G/T snv 1
rs202098093 1.000 0.040 1 151405476 missense variant G/A snv 1.2E-05 7.0E-06 1
rs370498156 1.000 0.040 1 151404903 missense variant T/C;G snv 4.0E-06 1.4E-05 1
rs373783340 1.000 0.040 1 151406243 missense variant G/A snv 4.0E-05 1.2E-04 1
rs375045125 1.000 0.040 1 151429672 missense variant T/C snv 4.0E-06 7.0E-06 1
rs548226228 1.000 0.040 1 151406914 missense variant G/A snv 1.2E-05 2.1E-05 1
rs561369202 1.000 0.040 1 151428152 missense variant T/C snv 6.4E-05 1.4E-05 1
rs574158925 1.000 0.040 1 151427829 missense variant T/C snv 5.6E-05 2.8E-05 1
rs574335012 1.000 0.040 1 151427959 missense variant G/C snv 1.2E-05 1
rs749270162 1.000 0.040 1 151406620 missense variant T/C snv 2.4E-05 1
rs749548928 1.000 0.040 1 151408815 missense variant T/C;G snv 4.0E-06 1
rs753214391 1.000 0.040 1 151406444 missense variant C/T snv 1.0E-05 2.1E-05 1
rs754532606 1.000 0.040 1 151423526 missense variant C/T snv 8.0E-06 2.1E-05 1
rs756691187 1.000 0.040 1 151404993 missense variant C/G snv 8.0E-06 7.0E-06 1
rs760059077 1.000 0.040 1 151405919 missense variant C/T snv 2.4E-05 2.1E-05 1
rs760211123 1.000 0.040 1 151405662 missense variant T/C snv 1.2E-05 7.0E-06 1
rs763820362 1.000 0.040 1 151424045 missense variant C/T snv 2.4E-05 1
rs769581210 1.000 0.040 1 151405376 missense variant T/C snv 7.2E-05 3.5E-05 1
rs772572695 1.000 0.040 1 151406427 missense variant C/A;T snv 2.5E-05 1
rs778792467 1.000 0.040 1 151405692 missense variant G/C snv 4.4E-05 7.0E-06 1
rs866632178 1.000 0.040 1 151441000 missense variant C/T snv 1.6E-05 1.4E-05 1