rs10838681, NR1H3

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 11 47253513 intron variant G/A snv 0.34 0.800 1.000 1 2012 2012
High density lipoprotein measurement
1440 1.000 0.040 11 47253513 intron variant G/A snv 0.34 0.700 1.000 1 2018 2018
Tonometry
CUI: C0040420
Disease: Tonometry
573 1.000 0.040 11 47253513 intron variant G/A snv 0.34 0.700 1.000 1 2018 2018