Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12601991 0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs11571818 0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs4808075 0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs11119608 0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20