Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 127
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 117
rs3856806
PPARG
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 12
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 10
rs2920502
PPARG
0.851 0.160 3 12287696 intron variant G/C snv 0.27 6
rs13306747
PPARG
0.807 0.200 3 12416775 synonymous variant C/A;G;T snv 8.0E-06; 4.2E-03; 7.2E-05 6
rs1175543
PPARG
0.851 0.120 3 12424934 intron variant A/G snv 0.28 5
rs1440763451
PPARG
0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs951599607
PPARG
0.925 0.040 3 12434028 missense variant G/A snv 4
rs780294601
PPARG
0.851 0.080 3 12416967 missense variant G/C snv 4.4E-05 1.4E-05 4
rs2972164
PPARG
0.925 0.080 3 12292917 intron variant T/C snv 0.46 3
rs72551364
PPARG
0.851 0.160 3 12433900 missense variant C/T snv 3
rs72551362
PPARG
0.925 0.080 3 12416836 missense variant G/A snv 4.0E-06 3
rs4684846
PPARG
0.882 0.080 3 12297350 intron variant A/G snv 0.28 3
rs2972162
PPARG
0.882 0.080 3 12383294 intron variant T/C snv 0.55 3
rs13073869
PPARG
0.882 0.080 3 12312494 intron variant G/A;C snv 3
rs4135247
PPARG
0.882 0.080 3 12355089 intron variant G/A;T snv 3
rs709151
PPARG
0.882 0.080 3 12413500 intron variant C/T snv 0.28 3
rs1899951
PPARG
0.851 0.160 3 12353341 intron variant C/T snv 0.26 3
rs709154
PPARG
0.925 0.200 3 12415335 intron variant A/T snv 0.28 2
rs9858822
PPARG
0.925 0.080 3 12369739 intron variant A/C snv 0.11 2
rs777334819
PPARG
0.925 0.120 3 12379856 missense variant G/A snv 3.6E-05 2.1E-05 2
rs9817428
PPARG
0.925 0.120 3 12298768 intron variant C/A snv 0.31 2
rs4135352
PPARG
0.925 0.120 3 12416709 missense variant C/G;T snv 2