Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107612 0.827 0.120 4 101818823 intron variant C/T snv 0.31 5
rs17199964 4 101786634 intron variant G/A;C snv 5
rs13126505 1.000 0.040 4 101944147 intron variant G/A snv 4.1E-02 3
rs10028805 0.882 0.160 4 101816093 intron variant G/A snv 0.45 3
rs34592089 1.000 0.040 4 102005766 intron variant G/A;T snv 2
rs71597109 0.925 0.120 4 101819845 intron variant C/T snv 0.27 2
rs17248480 4 101514108 intron variant G/A snv 1.8E-02 2
rs17031508 4 101639133 intron variant A/C snv 8.6E-02 1
rs10516491 4 102031709 intron variant T/C snv 6.5E-02 1
rs13127398 4 102000547 intron variant T/A snv 4.1E-02 1
rs4637409 1.000 0.080 4 101832251 intron variant A/G snv 0.27 1
rs4426778 1.000 0.080 4 101859567 intron variant G/A;C snv 1
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 1
rs17266594 0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs34061204 4 101878992 intron variant A/-;AA;AAA delins 1
rs6846071 4 101481058 intron variant T/G snv 0.15 1
rs13109404 4 101975434 intron variant T/G snv 4.1E-02 1