Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs156641 0.882 0.080 19 48128151 intron variant C/T snv 0.29 3
rs20579 0.882 0.080 19 48165573 5 prime UTR variant G/A;C snv 0.13 3
rs20581 0.882 0.080 19 48119170 synonymous variant A/G snv 0.58 0.64 3
rs3730859 0.882 0.080 19 48161802 intron variant G/A snv 0.30 3
rs439132 0.882 0.080 19 48165657 intron variant T/C snv 5.6E-02 9.6E-02 3
rs3730931 0.882 0.080 19 48143984 intron variant T/C snv 0.12 0.15 3