Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93 5
rs180327
BUD13
11 116752943 intron variant C/T snv 0.58 5
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 5
rs28927680
BUD13
11 116748357 3 prime UTR variant C/G;T snv 4
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3
rs3741300
BUD13
11 116760974 intron variant G/A snv 0.36 0.34 1
rs2075295
BUD13
11 116757685 intron variant T/C snv 0.31 1
rs4938310
BUD13
11 116759233 intron variant C/T snv 0.19 1
rs12292921
BUD13
11 116751247 intron variant T/G snv 0.10 1
rs11825181
BUD13
11 116755542 intron variant G/A snv 0.10 1
rs3825041
BUD13
11 116760991 intron variant T/A;C snv 0.89 1
rs6589564
BUD13
11 116753437 intron variant C/A;G snv 1
rs7930786
BUD13
11 116754011 intron variant C/G snv 0.92 1