Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894395 1.000 0.120 13 20189352 stop gained C/T snv 4.0E-06 1
rs1064797089 1.000 0.120 13 20189418 missense variant G/T snv 1
rs1064797090 1.000 0.120 13 20189410 missense variant G/A;C snv 1
rs111033186 1.000 0.120 13 20189125 missense variant C/T snv 9.3E-03 3.5E-03 1
rs111033217 1.000 0.120 13 20189538 missense variant T/G snv 1.2E-05 2.8E-05 1
rs111033296 1.000 0.120 13 20189463 missense variant G/C;T snv 4.0E-06 1
rs111033361 13 20189355 missense variant A/G snv 2.0E-05 7.0E-06 1
rs111033420 1.000 0.120 13 20189126 stop gained G/A;T snv 8.0E-06; 4.0E-06 1
rs117685390 1.000 0.120 13 20193170 upstream gene variant A/G snv 0.16 1
rs1422767764 1.000 0.120 13 20189283 missense variant T/A snv 1.6E-05 2.1E-05 1
rs1476034902 13 20189542 missense variant T/C snv 1.4E-05 1
rs150529554 13 20189227 stop gained C/A;T snv 4.0E-06; 1.0E-04 1
rs1555341783 1.000 0.120 13 20188911 frameshift variant TTTT/- delins 1
rs1555341794 1.000 0.120 13 20188937 frameshift variant A/- delins 1
rs1555341926 1.000 0.120 13 20189240 stop gained -/ACTC delins 1
rs1555341931 1.000 0.120 13 20189254 frameshift variant CC/T delins 1
rs1555341949 1.000 0.120 13 20189325 frameshift variant G/- del 1
rs1555341954 1.000 0.120 13 20189342 frameshift variant -/T delins 1
rs1555341957 1.000 0.120 13 20189346 missense variant A/C;G snv 1
rs1555341960 1.000 0.120 13 20189349 frameshift variant -/C delins 1
rs1555341993 1.000 0.120 13 20189451 frameshift variant AC/- delins 1
rs1555342007 1.000 0.120 13 20189532 frameshift variant AG/- delins 1
rs1555342014 1.000 0.120 13 20189571 frameshift variant C/- delins 1
rs1566528901 1.000 0.120 13 20189455 inframe deletion CCT/- delins 1
rs28931592 1.000 0.120 13 20189106 missense variant T/A snv 2.8E-05 2.8E-05 1