rs7841189, None

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.
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 1.000 0.040 8 19987865 TF binding site variant C/T snv 0.15 0.800 1.000 1 2012 2012
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 1.000 0.040 8 19987865 TF binding site variant C/T snv 0.15 0.700 1.000 1 2017 2017
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 0.040 8 19987865 TF binding site variant C/T snv 0.15 0.700 1.000 1 2012 2012