Gene: PPARG ×
Source: CLINVAR ×
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: rs1553638903
rs1553638903
PPARG
1 1.000 0.080 3 12349804 intron variant A/G snv 0.700 0
dbSNP: rs1553638909
rs1553638909
PPARG
1 1.000 0.080 3 12349824 intron variant A/T snv 0.700 0
dbSNP: rs948820149
rs948820149
PPARG
1 1.000 0.080 3 12350786 intron variant A/C;G snv 7.0E-06 0.700 0