Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs164147
NOS1AP
0.882 0.080 1 162368607 3 prime UTR variant A/C snv 0.76 3
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs8066560
SREBF1
0.925 0.040 17 17824729 intron variant A/G snv 0.64 2
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10139403
DLK1
1.000 0.040 14 100728224 intron variant A/G snv 0.62 1
rs1410713 1.000 0.040 20 3079704 downstream gene variant A/C snv 0.62 1
rs2282018
AVP
1.000 0.040 20 3084303 intron variant C/T snv 0.60 1
rs6084264
AVP
1.000 0.040 20 3089925 upstream gene variant T/C snv 0.58 1
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs10770125
INS-IGF2 ; IGF2 ; IGF2-AS
0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs2770381 1.000 0.040 20 3081340 downstream gene variant A/C snv 0.35 1
rs13412852
LPIN1
0.851 0.120 2 11774815 intron variant C/T snv 0.26 4
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs3738435
CHRM3
0.925 0.080 1 239907303 intron variant T/C snv 0.23 2
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs7744
MYD88
0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5