Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs191333060 1.000 0.040 X 100296405 missense variant G/A;C snv 1.3E-03 1
rs1555790846 1.000 0.040 20 8790220 missense variant C/T snv 1
rs202170644 1.000 0.040 3 64147176 missense variant C/G snv 4.7E-04 6.3E-04 1
rs145873257 1.000 0.040 16 7709117 missense variant G/A;T snv 1.8E-03 1
rs372761949 1.000 0.040 16 7595618 missense variant G/A snv 2.5E-05 1.4E-05 1
rs974157467 1.000 0.040 16 7676817 inframe insertion GCTGCC/-;GCTGCCGCTGCC delins 1
rs972548690 1.000 0.040 17 79094526 stop gained G/A;T snv 2.9E-05 1
rs114684479 1.000 0.040 7 103596518 missense variant G/T snv 1.6E-03 1.4E-03 1
rs369993428 1.000 0.040 7 103556983 missense variant T/C snv 4.0E-06 1
rs115035120 1.000 0.040 7 103483741 missense variant C/T snv 8.5E-04 2.9E-04 1
rs368906199 1.000 0.040 4 76213464 missense variant C/T snv 1.5E-04 9.1E-05 1
rs199692186 1.000 0.040 2 166272748 missense variant T/C snv 6.3E-04 5.5E-04 1
rs765818027 1.000 0.040 2 166293358 missense variant C/T snv 4.6E-05 2.8E-05 1
rs1553574522 1.000 0.040 2 165331362 missense variant T/C snv 1
rs200138205 1.000 0.040 2 165365200 missense variant G/A;C snv 1.7E-04; 3.2E-05 1
rs180922748 1.000 0.040 2 166233432 missense variant G/C snv 1.2E-03 1.7E-03 1
rs1555841977 1.000 0.040 21 6116503 missense variant C/T snv 1
rs1553155982 1.000 0.040 1 42928996 missense variant T/A snv 1
rs752396911 1.000 0.040 3 11025564 missense variant G/A;C;T snv 4.0E-05; 4.0E-06; 1.6E-05 1
rs202020647 1.000 0.040 1 37540752 missense variant G/A snv 1.8E-04 1.3E-04 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
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