Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 2
rs492602
LOC105447645 ; FUT2
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45 2