rs13226650, MLXIPL

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 7 73602675 intron variant A/G snv 0.19 0.800 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 0.040 7 73602675 intron variant A/G snv 0.19 0.700 1.000 1 2012 2012
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 1.000 0.040 7 73602675 intron variant A/G snv 0.19 0.700 1.000 1 2019 2019