PTGIR, prostaglandin I2 receptor, 5739

N. diseases: 27; N. variants: 4
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4987262
rs4987262
0.882 0.040 19 46623592 missense variant G/A;C snv 7.1E-03
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.010 1.000 1 2008 2008