Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10038162 1.000 0.040 5 138901066 intron variant G/A snv 0.31 1
rs10043478 1.000 0.040 5 138853022 intron variant G/C snv 0.67 1
rs10515504 1.000 0.040 5 138887305 intron variant C/G snv 0.30 1
rs11749163 1.000 0.040 5 138926981 intron variant A/G;T snv 0.30 1
rs13171173 1.000 0.040 5 138706775 intron variant G/C;T snv 1
rs13177415 1.000 0.040 5 138914251 intron variant C/A;T snv 1
rs160399 1.000 0.040 5 138727552 intron variant A/C;G snv 1
rs160400 1.000 0.040 5 138727330 intron variant C/T snv 0.36 1
rs160401 1.000 0.040 5 138725652 intron variant T/C snv 0.31 1
rs17031 1.000 0.040 5 138934853 3 prime UTR variant T/A;C snv 1
rs17207681 1.000 0.040 5 138832838 intron variant A/G snv 7.3E-02 1
rs17286171 1.000 0.040 5 138719619 intron variant C/T snv 0.12 1
rs176382 1.000 0.040 5 138891078 intron variant T/C snv 0.33 1
rs1828187 1.000 0.040 5 138836531 intron variant C/T snv 0.67 1
rs288016 1.000 0.040 5 138859299 intron variant C/T snv 0.69 1
rs288018 1.000 0.040 5 138856727 intron variant G/A snv 0.74 1
rs288028 1.000 0.040 5 138886300 splice region variant G/C snv 0.27 0.26 1
rs288029 1.000 0.040 5 138881616 intron variant T/C snv 0.24 1
rs288033 1.000 0.040 5 138878405 intron variant T/C snv 0.36 1
rs311596 1.000 0.040 5 138736393 intron variant A/T snv 0.30 1
rs3763016 1.000 0.040 5 138935043 downstream gene variant C/G snv 0.36 1
rs825669 1.000 0.040 5 138731258 intron variant A/T snv 0.33 1
rs825672 1.000 0.040 5 138759954 intron variant T/C snv 0.74 1
rs825747 1.000 0.040 5 138800896 intron variant G/A snv 0.74 1
rs906695 1.000 0.040 5 138803588 intron variant C/T snv 0.68 1