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: rs2075650
rs2075650 		0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.800 1.000 5 2008 2019
dbSNP: rs2075650
rs2075650 		0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 5 2008 2013
dbSNP: rs2075650
rs2075650 		0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 4 2008 2013
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: rs2075650
rs2075650 		0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.900 1.000 33 2009 2020
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: rs8106922
rs8106922 		1.000 0.080 19 44898409 intron variant A/G snv 0.36
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.800 1.000 10 2009 2019
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
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: rs2075650
rs2075650 		0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 3 2009 2013
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: 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: rs10524523
rs10524523 		0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		Nervous System Diseases; Mental Disorders 0.080 0.875 8 2010 2017
dbSNP: rs157582
rs157582 		0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.810 1.000 7 2010 2019
dbSNP: rs405697
rs405697 		1.000 0.080 19 44901434 3 prime UTR variant A/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.800 1.000 4 2011 2019
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: 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