Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607906 1.000 0.160 3 37050576 stop gained A/C;G;T snv 1
rs35045067 0.925 0.160 3 37048557 missense variant A/C;G snv 4.4E-05 1
rs41295282 1.000 0.160 3 37001024 missense variant A/G snv 1.6E-05 7.0E-05 1
rs41295284 0.925 0.160 3 37047607 missense variant T/A snv 1.9E-04 1.5E-04 1
rs587778964 0.882 0.160 3 37048604 missense variant A/C;T snv 1
rs63750511 0.925 0.160 3 37040252 missense variant A/C;T snv 1
rs63750710 0.925 0.160 3 37020411 missense variant A/C snv 1
rs63750781 0.851 0.160 3 37004444 missense variant C/G;T snv 4.0E-06 1
rs63751094 0.925 0.160 3 36996624 stop lost A/G;T snv 1
rs63751428 0.882 0.160 3 36996686 stop gained C/A;T snv 1
rs63751608 0.925 0.160 3 37042321 missense variant T/C snv 1
rs63751615 0.851 0.200 3 37012098 stop gained C/A;T snv 4.0E-06 1
rs63751713 0.925 0.160 3 37047531 missense variant C/G;T snv 1
rs1060504000 0.925 0.160 3 37025666 missense variant T/C snv 2
rs1260021106 0.925 0.160 3 37025645 missense variant A/G snv 1.6E-05 2
rs1392665848 0.925 0.160 3 37025865 missense variant A/G snv 4.0E-06 2
rs587778914 0.925 0.160 3 36996645 missense variant A/C snv 2
rs587778992 0.882 0.200 3 37050606 stop gained C/T snv 2
rs63749818 0.925 0.160 3 37007002 stop gained C/A;G;T snv 2
rs63749820 0.882 0.200 3 37007046 stop gained C/T snv 2
rs63749939 0.851 0.160 3 36996702 missense variant G/A snv 2
rs63750211 0.882 0.160 3 37008904 missense variant A/G snv 2
rs63750693 0.882 0.160 3 37047652 missense variant T/A;C snv 2
rs63750791 0.925 0.160 3 37025864 synonymous variant C/T snv 1.8E-04 2.1E-05 2
rs786201226 0.925 0.160 3 37014450 synonymous variant A/G;T snv 4.0E-06 2