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
rs886041065
ASXL2
0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs5742612
LOC105369944 ; IGF1
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 10
rs587777732
MIR3646 ; HNF4A
0.763 0.240 20 44406195 missense variant C/T snv 9
rs1057515572
PMS2
0.882 0.200 7 5987033 frameshift variant GC/ACT delins 8
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 8
rs2920502
PPARG
0.851 0.160 3 12287696 intron variant G/C snv 0.27 6
rs1057518775
KCNJ11
0.851 0.160 11 17387907 missense variant G/A;C snv 4
rs121909730
GLUD1
0.882 0.040 10 87053380 missense variant G/A snv 4
rs2014355
ACADS
0.925 0.120 12 120737721 non coding transcript exon variant T/C snv 0.22 4
rs9402571 0.882 0.080 6 134167822 downstream gene variant T/G snv 0.22 4
rs1003887
INSL3
0.882 0.240 19 17816591 3 prime UTR variant C/T snv 0.69 3
rs12143966
NLRP3
1.000 0.040 1 247438055 intron variant G/A snv 0.33 2
rs225017
DIO2
0.925 0.080 14 80200883 3 prime UTR variant A/T snv 0.58 2
rs2288377
LOC105369944 ; IGF1
0.925 0.080 12 102480984 intron variant A/G;T snv 2
rs2918419
NR3C1
0.925 0.040 5 143342788 intron variant T/C snv 0.15 2
rs4629571
CERT1 ; HMGCR
0.925 0.160 5 75362479 intron variant A/G snv 8.7E-02 2