Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1635852 0.882 0.160 7 28149792 intron variant T/C snv 0.42 4
rs1708299 7 28150327 intron variant A/G snv 0.77 2
rs508347 7 28173205 intron variant T/C snv 0.69 2
rs552707 7 28165684 intron variant T/C snv 0.77 2
rs1029534 7 28149464 intron variant T/C;G snv 1
rs1557779 7 27955139 intron variant T/C snv 0.85 1
rs1635851 7 28148187 intron variant C/T snv 0.55 1
rs73091214 7 28160705 intron variant T/C snv 7.0E-02 1
rs849141 0.851 0.240 7 28145472 intron variant A/G snv 0.78 1