Gene: PPARG ×
Source: GWASCAT ×
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: rs1801282
rs1801282
PPARG
5 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.900 0.902 4 1997 2018
dbSNP: rs1899951
rs1899951
PPARG
2 0.851 0.160 3 12353341 intron variant C/T snv 0.26 0.800 1.000 1 2012 2018
dbSNP: rs11709077
rs11709077
PPARG
3 0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs17036160
rs17036160
PPARG
1 1.000 0.080 3 12288284 intron variant C/T snv 8.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs3963364
rs3963364
PPARG
1 1.000 0.080 3 12343858 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs4684848
rs4684848
PPARG
1 1.000 0.080 3 12354146 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs71304101
rs71304101
PPARG
1 1.000 0.080 3 12355414 intron variant G/A snv 9.2E-02 0.700 1.000 1 2018 2018