rs4788815, LOC105371334

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 16 71600908 intergenic variant A/T snv 0.69 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 16 71600908 intergenic variant A/T snv 0.69 0.700 1.000 1 2012 2012
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 16 71600908 intergenic variant A/T snv 0.69 0.700 1.000 1 2019 2019