Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs766432
BCL11A
0.925 0.080 2 60492835 intron variant C/A snv 0.80 6
rs35152987
HBD
0.925 0.080 11 5234352 missense variant C/A;T snv 2.2E-03 4
rs7950726 11 5204217 upstream gene variant C/A snv 0.17 1