Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 80
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 79
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 54
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 44
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 27
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 26
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 25
rs4778889
IL16
0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 23
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 20
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 18
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 18
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 18
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 17
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 16
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs184003
AGER
0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 15
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 14
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 14
rs2072668
OGG1
0.732 0.280 3 9756456 intron variant C/G snv 0.28 0.24 14