Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs13339636
FAM234A
16 248589 intron variant A/G snv 3.8E-02 5
rs13335629
FAM234A
16 260381 intron variant G/A;C snv 1.1E-02 4
rs3743879
RGS11 ; FAM234A
16 268475 3 prime UTR variant C/A;G snv 2