Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13428113
LOC107985940 ; INSIG2
1.000 0.040 2 118089309 intron variant T/C snv 0.51 1
rs9308762
INSIG2
0.925 0.120 2 118106298 intron variant C/A;G;T snv 2
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs2920502
PPARG
0.851 0.160 3 12287696 intron variant G/C snv 0.27 6
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs7649970
PPARG
1.000 0.040 3 12350773 intron variant C/T snv 0.14 2
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs3856806
PPARG
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2980888 1.000 0.040 8 125495066 intron variant T/C snv 0.76 2
rs11794552
LOC105376299 ; PLPP7
1.000 0.040 9 131344938 intron variant C/T snv 0.15 1
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs2668423
PWWP3A
1.000 0.040 19 1370527 intron variant T/G snv 0.73 1
rs11166927
TRAPPC9
1.000 0.040 8 139784177 intron variant T/C snv 0.39 1
rs17107315
SPINK1
0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs3772633
AGTR1
1.000 0.040 3 148700381 intron variant T/C snv 0.13 1
rs2276736
AGTR1
1.000 0.040 3 148708086 intron variant A/G;T snv 1
rs3772630
AGTR1
1.000 0.040 3 148708685 intron variant T/C snv 0.44 1
rs2638360
AGTR1
0.925 0.080 3 148710569 intron variant G/A;T snv 3
rs3772627
AGTR1
1.000 0.040 3 148712467 intron variant A/G snv 0.44 1