Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12646351 0.790 0.080 4 145819473 intron variant G/A snv 0.19 10
rs17806780 0.790 0.080 4 145811502 intron variant T/C snv 0.18 10
rs4835265 4 145900258 intron variant C/A snv 0.15 6
rs11930385 4 145924600 intron variant C/T snv 0.51 1
rs12331851 1.000 0.040 4 145928143 intron variant G/A snv 7.1E-02 1
rs2048161 4 145932013 intron variant A/C;G snv 1
rs35146602 4 145866089 intron variant A/G snv 0.15 1
rs35879803 1.000 0.040 4 145861685 non coding transcript exon variant C/A;T snv 1
rs4345206 1.000 0.040 4 145845384 intron variant T/C snv 0.59 1
rs4547811 4 145873469 intron variant T/C snv 0.20 1
rs4835266 4 145900573 intron variant T/A;C snv 1
rs7666150 4 145893488 intron variant T/C snv 0.54 1