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: rs1160985
rs1160985 		1.000 0.080 19 44900155 intron variant C/T snv 0.52
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 3 2013 2019
dbSNP: rs1160985
rs1160985 		1.000 0.080 19 44900155 intron variant C/T snv 0.52
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.800 1.000 2 2013 2019
dbSNP: rs1160985
rs1160985 		1.000 0.080 19 44900155 intron variant C/T snv 0.52
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2013 2019
dbSNP: rs1160985
rs1160985 		1.000 0.080 19 44900155 intron variant C/T snv 0.52
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.800 1.000 2 2012 2019
dbSNP: rs1160985
rs1160985 		1.000 0.080 19 44900155 intron variant C/T snv 0.52
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1160985
rs1160985 		1.000 0.080 19 44900155 intron variant C/T snv 0.52
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.700 1.000 1 2013 2013
dbSNP: rs11668327
rs11668327 		1.000 0.080 19 44895376 intron variant G/C snv 0.12
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs11668327
rs11668327 		1.000 0.080 19 44895376 intron variant G/C snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs117310449
rs117310449 		1.000 0.080 19 44890259 intron variant C/T snv 7.3E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs141864196
rs141864196 		1.000 0.080 19 44902242 3 prime UTR variant G/A snv 1.7E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 2 2018 2019
dbSNP: rs142412517
rs142412517 		1.000 0.080 19 44900801 missense variant C/T snv 4.9E-04 5.7E-04
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.810 1.000 14 2009 2019
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 3 2009 2012
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 3 2009 2012
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2012 2019
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2014 2014
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		Respiratory Tract Diseases; Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2013 2013
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0019348
Disease: Herpes Simplex Infections
Herpes Simplex Infections 		Infections; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement 		0.700 1.000 1 2009 2009
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2009 2009
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2009 2009
dbSNP: rs157580
rs157580 		0.882 0.160 19 44892009 intron variant G/A snv 0.69
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012