Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs80356616
KCNJ11
0.732 0.360 11 17387917 missense variant C/T snv 19
rs80356624
KCNJ11
0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs137853240
HNF1A
0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs80356618
KCNJ11
0.807 0.200 11 17387595 missense variant C/A;T snv 8
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 7
rs518147
HTR2C
0.807 0.200 X 114584109 5 prime UTR variant C/A;G snv 7
rs137853238
HNF1A
0.807 0.200 12 120994265 missense variant G/A snv 6
rs267607555
LMNA
0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 6
rs7744
MYD88
0.827 0.160 3 38142530 3 prime UTR variant A/G snv 0.13 5
rs12836771
HTR2C ; MIR1912 ; MIR1264
0.882 0.080 X 114650913 intron variant A/G snv 0.12 4
rs13412852
LPIN1
0.851 0.120 2 11774815 intron variant C/T snv 0.26 4