Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16953946 16 80751551 intron variant T/A;C snv 1
rs8063688 16 80603118 3 prime UTR variant A/G snv 0.53 1
rs13329835 0.925 0.080 16 80616908 intron variant A/G snv 0.35 1
rs72820985 1.000 0.080 16 80805081 upstream gene variant A/G snv 0.17 1
rs7500067 1.000 0.080 16 80614399 intron variant A/G snv 0.24 1
rs4613079 16 80610060 intron variant G/A snv 4.2E-02 1