Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11023906 11 16302860 intron variant G/A snv 0.17 3
rs12799126 11 16286917 intron variant G/T snv 0.17 3
rs1156725 11 16286154 intron variant C/T snv 0.78 2
rs1401454 11 16228637 intron variant C/A;G;T snv 2
rs2014408 11 16343736 intron variant C/T snv 0.17 2
rs2218001 11 16320669 intron variant A/C;G;T snv 2
rs4757391 11 16281393 intron variant C/T snv 0.78 2
rs10832586 11 16282543 intron variant A/C;T snv 1