MLXIPL, MLX interacting protein like, 51085

N. diseases: 165; N. variants: 29
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1051921
rs1051921 		0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 2 2019 2019
dbSNP: rs1051921
rs1051921 		0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1051921
rs1051921 		0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1051921
rs1051921 		0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1051921
rs1051921 		0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1051921
rs1051921 		0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1051921
rs1051921 		0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15
CUI: C0018099
Disease: Gout
Gout 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1051921
rs1051921 		0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018
dbSNP: rs13247874
rs13247874 		7 73596112 intron variant C/T snv 0.15 0.15
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2012
dbSNP: rs35332062
rs35332062 		7 73597712 missense variant G/A snv 0.10 0.10
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35332062
rs35332062 		7 73597712 missense variant G/A snv 0.10 0.10
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs79624003
rs79624003 		7 73598455 intron variant A/G snv 0.10
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2019 2019
dbSNP: rs79624003
rs79624003 		7 73598455 intron variant A/G snv 0.10
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs79624003
rs79624003 		7 73598455 intron variant A/G snv 0.10
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs13235543
rs13235543 		7 73599571 synonymous variant C/G;T snv 0.11 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13240065
rs13240065 		7 73601039 intron variant G/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34346326
rs34346326 		7 73601851 intron variant T/C snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs56383788
rs56383788 		7 73602070 intron variant A/G snv 1.8E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13240994
rs13240994 		7 73602532 intron variant T/C snv 0.16
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs13240994
rs13240994 		7 73602532 intron variant T/C snv 0.16
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs13226650
rs13226650 		1.000 0.040 7 73602675 intron variant A/G snv 0.19
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.800 1.000 1 2012 2012
dbSNP: rs13226650
rs13226650 		1.000 0.040 7 73602675 intron variant A/G snv 0.19
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13226650
rs13226650 		1.000 0.040 7 73602675 intron variant A/G snv 0.19
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs35368205
rs35368205 		7 73603327 intron variant C/T snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34166762
rs34166762 		7 73604194 intron variant T/C snv 0.31
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019