Gene: PPARG ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800571
rs1800571
PPARG
2 0.925 0.080 3 12381349 missense variant C/A snv 1.4E-05 0.700 0
dbSNP: rs1801282
rs1801282
PPARG
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.100 0.804 46 1997 2018
dbSNP: rs1805192
rs1805192
PPARG
121 0.510 0.840 3 12379739 missense variant C/G snv 0.100 0.837 43 1997 2018
dbSNP: rs3856806
rs3856806
PPARG
41 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.070 0.857 7 2005 2017
dbSNP: rs10865710
rs10865710
PPARG
13 0.763 0.360 3 12311699 intron variant C/G snv 0.25 0.010 1.000 1 2018 2018
dbSNP: rs13306747
rs13306747
PPARG
6 0.807 0.200 3 12416775 synonymous variant C/A;G;T snv 8.0E-06; 4.2E-03; 7.2E-05 0.010 1.000 1 2005 2005
dbSNP: rs1354592503
rs1354592503
PPARG
2 0.925 0.120 3 12381463 missense variant A/G snv 1.4E-05 0.010 1.000 1 2011 2011
dbSNP: rs1822825
rs1822825
PPARG
2 0.925 0.080 3 12408464 intron variant G/A snv 0.61 0.010 1.000 1 2013 2013
dbSNP: rs4135352
rs4135352
PPARG
2 0.925 0.120 3 12416709 missense variant C/G;T snv 0.010 1.000 1 2014 2014