rs2657880, SPRYD4

N. diseases: 4
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 12 56469986 3 prime UTR variant G/C snv 0.15 0.700 1.000 1 2012 2012
Lymphocyte Count measurement
CUI: C0200635
Disease: Lymphocyte Count measurement
456 12 56469986 3 prime UTR variant G/C snv 0.15 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 12 56469986 3 prime UTR variant G/C snv 0.15 0.700 1.000 1 2012 2012
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 12 56469986 3 prime UTR variant G/C snv 0.15 0.700 1.000 1 2018 2018