Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4894797 3 172065756 intron variant G/A snv 0.47 2
rs11718418 3 172053964 intron variant A/G snv 0.55 1
rs4243400 3 172253069 intron variant A/G snv 0.60 1
rs4535251 3 172208583 intron variant T/A;C snv 1
rs4894539 3 172281493 intron variant G/T snv 0.53 1
rs62281815 3 172252520 intron variant A/T snv 0.41 1
rs7652177 3 172251287 missense variant C/G snv 0.54 0.61 1