Source: ALL

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-02 131
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
rs121909242
PPARG
0.925 0.080 3 12416825 missense variant A/C snv 2
rs28936407
PPARG
0.925 0.080 3 12416831 missense variant G/A snv 8.0E-06 2.1E-05 2
rs9858822
PPARG
0.925 0.080 3 12369739 intron variant A/C snv 0.11 2
rs121909243
PPARG
1.000 0.080 3 12416923 stop gained A/T snv 1
rs587776687
PPARG
1.000 0.080 3 12392683 frameshift variant A/- delins 1