Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7124972 11 81291756 intron variant C/T snv 7.7E-02 1
rs7704641 5 5260570 intron variant G/A snv 0.37 1
rs4767841
CIT
12 119724394 intron variant G/A snv 0.55 1
rs150663673 10 25118280 intron variant G/A snv 1.3E-02 1
rs112673195 12 31908519 intron variant G/A;C snv 1
rs72881251 18 25094696 intron variant T/C snv 0.14 1