Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1801282
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.050 1.000 5 2008 2014
dbSNP: rs1805192
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.040 1.000 4 2008 2012
dbSNP: rs145566594
rs145566594
PPARG
1.000 0.040 3 12416950 missense variant A/C;G snv 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2018 2018