Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3923809 1.000 0.080 6 38473194 intron variant A/G snv 0.32 1
rs4236060 1.000 0.080 6 38502311 intron variant C/T snv 0.22 1
rs4714156 0.925 0.120 6 38393336 intron variant C/T snv 0.36 1
rs6904723 1.000 0.080 6 38468541 intron variant A/C;T snv 1
rs6923737 1.000 0.080 6 38515788 intron variant T/C snv 0.28 1
rs9296249 0.882 0.120 6 38398065 intron variant T/C snv 0.30 1
rs9357271 0.776 0.160 6 38398097 intron variant T/C snv 0.38 1