Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs766432
BCL11A
0.925 0.080 2 60492835 intron variant C/A snv 0.80 5
rs2071348
HBD ; HBBP1
1.000 0.080 11 5242916 intron variant T/G snv 0.25 1
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 1