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: rs72551363
rs72551363
PPARG
3 0.882 0.080 3 12417048 missense variant T/A snv 0.800 1.000 2 2002 2002
dbSNP: rs72551364
rs72551364
PPARG
4 0.851 0.160 3 12433900 missense variant C/T snv 0.800 1.000 2 2002 2002
dbSNP: rs121909244
rs121909244
PPARG
11 0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 0.700 1.000 4 2000 2014
dbSNP: rs121909245
rs121909245
PPARG
2 0.925 0.080 3 12392701 missense variant T/A snv 0.700 0
dbSNP: rs121909246
rs121909246
PPARG
1 1.000 0.080 3 12392713 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs1378972597
rs1378972597
PPARG
1 1.000 0.080 3 12416855 missense variant T/C snv 4.0E-06 0.700 0
dbSNP: rs148195788
rs148195788
PPARG
1 1.000 0.080 3 12392714 missense variant G/A snv 0.700 0
dbSNP: rs1553643326
rs1553643326
PPARG
1 1.000 0.080 3 12381481 missense variant A/G snv 0.700 0
dbSNP: rs1553647989
rs1553647989
PPARG
1 1.000 0.080 3 12405897 missense variant G/A snv 0.700 0
dbSNP: rs1553650477
rs1553650477
PPARG
1 1.000 0.080 3 12416893 frameshift variant CTTGA/- delins 0.700 0
dbSNP: rs1553653993
rs1553653993
PPARG
1 1.000 0.080 3 12433979 missense variant T/C snv 0.700 0
dbSNP: rs72551362
rs72551362
PPARG
4 0.925 0.080 3 12416836 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs770557781
rs770557781
PPARG
1 1.000 0.080 3 12433986 frameshift variant C/- delins 8.0E-06 0.700 0