Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4253421
F11
4 186283783 intron variant A/C;G;T snv 2
rs2289252 1.000 0.040 4 186286227 non coding transcript exon variant C/T snv 0.35 2
rs1593
F11
4 186274397 3 prime UTR variant T/A;G snv 1
rs56810541
F11
4 186279396 intron variant A/T snv 0.35 1