Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1040558 1.000 0.080 6 20713475 intron variant A/G snv 0.19 1
rs10440833 1.000 0.080 6 20687890 intron variant T/A;G snv 0.26 1
rs10946398 0.827 0.160 6 20660803 intron variant A/C snv 0.40 3
rs10946403 1.000 0.080 6 20717173 intron variant A/G snv 0.30 1
rs10946406 1.000 0.080 6 20758529 intron variant A/G;T snv 1
rs11753081 1.000 0.080 6 20705359 intron variant T/G snv 0.19 1
rs12111351 1.000 0.080 6 20724327 intron variant T/G snv 0.34 1
rs12664021 1.000 0.080 6 20760849 intron variant C/T snv 0.11 1
rs145494032 1.000 0.080 6 20665715 intron variant -/C delins 4.9E-05 1
rs1569699 1.000 0.080 6 20679079 intron variant T/G snv 0.41 1
rs2206734 0.882 0.160 6 20694653 intron variant C/T snv 0.20 3
rs2328529 1.000 0.080 6 20631722 intron variant C/A snv 0.19 1
rs2328531 1.000 0.080 6 20643521 intron variant A/G;T snv 1
rs2328545 1.000 0.080 6 20653319 intron variant G/A;C snv 1
rs2328548 1.000 0.080 6 20716727 intron variant G/A;T snv 1
rs2820001 1.000 0.080 6 20758712 intron variant G/T snv 0.85 1
rs4235999 1.000 0.080 6 20642991 intron variant C/G;T snv 0.39 1
rs4493738 1.000 0.080 6 20775429 intron variant A/G snv 7.5E-02 1
rs4710938 1.000 0.080 6 20640673 intron variant A/G snv 0.42 1
rs4710939 1.000 0.080 6 20644713 intron variant A/G snv 0.41 1
rs4710940 1.000 0.080 6 20657781 intron variant A/C snv 0.46 1
rs4712522 1.000 0.080 6 20656569 intron variant C/G snv 0.40 1
rs4712523 0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs4712524 0.925 0.120 6 20657634 intron variant A/G snv 0.40 2
rs4712525 1.000 0.080 6 20662735 intron variant C/G;T snv 1