Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 21
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 20
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 18
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 18
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 17
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 17
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 17
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs199474657
TRNL1 ; ND1 ; ND2
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv 15
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 15
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 15
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 14