Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4458523
WFS1
1.000 0.080 4 6288259 intron variant T/G snv 0.61 3
rs4689388
WFS1
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 3
rs1801214
WFS1
1.000 0.080 4 6301295 missense variant C/A;G;T snv 0.67 1
rs4416547
WFS1
1.000 0.080 4 6292240 intron variant G/A snv 0.63 1
rs4688985
WFS1
1.000 0.080 4 6283988 intron variant A/G snv 0.79 1