Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115035120 1.000 0.040 7 103483741 missense variant C/T snv 8.5E-04 2.9E-04 1
rs200124755 1.000 0.040 7 103498074 splice region variant T/G snv 5.2E-04 2.9E-04 1
rs369675346 1.000 0.040 7 147120974 splice region variant C/A;T snv 8.0E-06; 2.7E-04 1
rs369993428 1.000 0.040 7 103556983 missense variant T/C snv 4.0E-06 1
rs751409835 1.000 0.040 7 103486204 stop gained G/A;C snv 1.2E-05 1
rs758630057 1.000 0.040 7 148147587 missense variant G/A snv 4.7E-04 4.7E-04 1
rs61738009 0.827 0.080 8 67483807 stop gained C/A;T snv 4.0E-06; 2.0E-03 2.5E-03 11
rs35993949 0.882 0.040 8 67506804 missense variant G/C snv 1.5E-03 1.2E-03 9
rs118192247 0.882 0.080 8 132175491 missense variant C/T snv 3
rs1381851622 1.000 0.040 8 132174283 missense variant C/T snv 1.9E-05 1
rs147896487 1.000 0.040 8 18084767 missense variant C/G snv 1.3E-03 1.5E-03 1
rs150821246 1.000 0.040 8 132129618 missense variant C/T snv 3.7E-04 3.1E-04 1
rs1554626549 1.000 0.040 8 132170427 missense variant G/A snv 1
rs138282349 1.000 0.040 9 135792094 missense variant G/A snv 1.0E-03 1.2E-03 1
rs143166100 1.000 0.040 9 128607988 missense variant C/G snv 5.7E-04 5.4E-04 1
rs1441152520 1.000 0.040 9 128632218 missense variant A/G snv 1
rs1554759745 1.000 0.040 9 128611792 missense variant G/A snv 1
rs1554770659 1.000 0.040 9 137163819 missense variant T/C snv 1
rs569997507 1.000 0.040 9 128604371 missense variant C/T snv 4.0E-05 4.2E-05 1
rs780658554 1.000 0.040 9 128584312 missense variant C/T snv 3.2E-05 3.5E-05 1
rs1555437424 1.000 0.040 15 92924407 missense variant G/A snv 1
rs1555445693 1.000 0.040 15 93014832 missense variant C/T snv 1
rs755898320 1.000 0.040 15 93009265 missense variant C/T snv 2.0E-05 6.3E-05 1
rs765965968 0.882 0.080 16 2498333 missense variant G/A;T snv 1.3E-05; 4.2E-06 5
rs1250662891 0.925 0.040 16 10180176 missense variant G/C snv 4.0E-06 2