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: 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: 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
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: rs2075650
rs2075650
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2009 2009
dbSNP: rs2075650
rs2075650
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0007273
Disease: Carotid Artery Diseases
Carotid Artery Diseases
Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs8106922
rs8106922
1.000 0.080 19 44898409 intron variant A/G snv 0.36
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement
0.700 1.000 1 2009 2009
dbSNP: rs10119
rs10119
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 < 0.001 1 2011 2011
dbSNP: rs11556510
rs11556510
1.000 0.040 19 44891562 missense variant T/G snv 9.8E-03 1.2E-02
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 < 0.001 1 2011 2011
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: rs2075650
rs2075650
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs2075650
rs2075650
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs59007384
rs59007384
0.851 0.080 19 44893408 intron variant G/A;T snv
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
Mental Disorders 0.010 < 0.001 1 2011 2011
dbSNP: rs10119
rs10119
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.700 1.000 3 2009 2012
dbSNP: rs157580
rs157580
0.882 0.160 19 44892009 intron variant G/A snv 0.69
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: rs2075650
rs2075650
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0023980
Disease: Longevity
Longevity
0.800 1.000 2 2011 2012
dbSNP: rs10119
rs10119
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs11556505
rs11556505
0.925 0.080 19 44892887 synonymous variant C/T snv 0.13 0.13
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
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: 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: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs157581
rs157581
0.925 0.080 19 44892457 synonymous variant T/C snv 0.25 0.29
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs157582
rs157582
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29
CUI: C0349198
Disease: Acute transient psychotic disorder
Acute transient psychotic disorder
Pathological Conditions, Signs and Symptoms; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs157582
rs157582
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.800 1.000 1 2012 2012