Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2667978
LYN
1.000 0.080 8 55985392 intron variant A/G snv 0.18 1
rs7829816
LYN
1.000 0.080 8 55936827 intron variant A/G snv 0.27 1