Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs59616136 19 17141231 intron variant G/A snv 8.1E-02 4
rs11881955 19 17143698 intron variant A/G snv 0.49 2
rs35365035 19 17141341 intron variant T/C snv 0.49 2
rs4808579 19 17144924 intron variant T/A;C snv 2