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: 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: rs8106922
rs8106922 		1.000 0.080 19 44898409 intron variant A/G snv 0.36
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 3 2012 2019
dbSNP: rs8106922
rs8106922 		1.000 0.080 19 44898409 intron variant A/G snv 0.36
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2018 2019
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: rs8106922
rs8106922 		1.000 0.080 19 44898409 intron variant A/G snv 0.36
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs77301115
rs77301115 		1.000 0.080 19 44893716 intron variant G/A snv 2.8E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs77301115
rs77301115 		1.000 0.080 19 44893716 intron variant G/A snv 2.8E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs76692773
rs76692773 		1.000 0.080 19 44890954 intron variant C/T snv 7.5E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs76366838
rs76366838 		19 44896639 intron variant G/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs760136
rs760136 		1.000 0.080 19 44900601 intron variant A/G snv 0.52
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.800 1.000 2 2013 2018
dbSNP: rs741780
rs741780 		1.000 0.080 19 44901174 intron variant T/C snv 0.47 0.52
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs71352238
rs71352238 		1.000 0.080 19 44891079 intron variant T/C snv 0.10
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs61679753
rs61679753 		1.000 0.080 19 44897490 intron variant T/A snv 5.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs61679753
rs61679753 		1.000 0.080 19 44897490 intron variant T/A snv 5.6E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs59007384
rs59007384 		0.851 0.080 19 44893408 intron variant G/A;T snv
CUI: C0014544
Disease: Epilepsy
Epilepsy 		Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs59007384
rs59007384 		0.851 0.080 19 44893408 intron variant G/A;T snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		Nervous System Diseases 0.010 1.000 1 2015 2015
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: rs59007384
rs59007384 		0.851 0.080 19 44893408 intron variant G/A;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs561654715
rs561654715 		1.000 0.080 19 44890947 intron variant G/A snv 1.7E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 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: rs394819
rs394819 		1.000 0.080 19 44901322 missense variant G/A;T snv 3.7E-05; 9.7E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs35568738
rs35568738 		1.000 0.080 19 44899461 intron variant G/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs34404554
rs34404554 		1.000 0.080 19 44892652 intron variant C/G snv 0.12
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs34404554
rs34404554 		1.000 0.080 19 44892652 intron variant C/G snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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