Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs3135002 1.000 0.120 6 32700662 TF binding site variant A/C snv 0.80 2
rs559047 1.000 0.120 1 238590616 intergenic variant T/A;C snv 2
rs61211515 1.000 0.120 6 30133199 upstream gene variant TT/-;T;TTT;TTTT delins 0.14 2
rs9260151
HLA-A
1.000 0.120 6 29943253 non coding transcript exon variant C/T snv 0.16 0.14 2
rs6517656
BACE2
21 41211811 intron variant G/A snv 0.34 1