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
rs9924561
FAM234A
16 264781 intron variant G/A;T snv 2.9E-05; 6.5E-03 3
rs4374177
FAM234A
16 256244 intron variant A/G snv 0.25 1
rs533614130
FAM234A
16 236001 intron variant A/G snv 3.4E-04 1
rs7189020
FAM234A
16 254804 intron variant A/T snv 0.55 1