rs10119
|
0.925 |
0.080 |
19 |
44903416 |
3 prime UTR variant |
G/A
|
snv
|
|
0.28
|
Mild cognitive disorder
|
Mental Disorders
|
0.010 |
< 0.001 |
1 |
2011 |
2011 |
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
|
|
|
Diabetes Mellitus, Non-Insulin-Dependent
|
Nutritional and Metabolic Diseases; Endocrine System Diseases
|
0.010 |
1.000 |
1 |
2014 |
2014 |
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
|
|
|
Mental deterioration
|
Mental Disorders
|
0.010 |
1.000 |
1 |
2017 |
2017 |
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
|
|
|
Familial Alzheimer Disease (FAD)
|
Nervous System Diseases; Mental Disorders
|
0.010 |
1.000 |
1 |
2013 |
2013 |
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
|
|
|
Inclusion Body Myopathy, Sporadic
|
Musculoskeletal Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs10527454
|
1.000 |
0.080 |
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
|
|
|
Inclusion Body Myopathy, Sporadic
|
Musculoskeletal Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs11556505
|
0.925 |
0.080 |
19 |
44892887 |
synonymous variant |
C/T
|
snv
|
0.13
|
0.13
|
Alzheimer Disease, Late Onset
|
Nervous System Diseases; Mental Disorders
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs11556510
|
1.000 |
0.040 |
19 |
44891562 |
missense variant |
T/G
|
snv
|
9.8E-03
|
1.2E-02
|
Mild cognitive disorder
|
Mental Disorders
|
0.010 |
< 0.001 |
1 |
2011 |
2011 |
rs115881343
|
1.000 |
0.040 |
19 |
44899959 |
intron variant |
C/G;T
|
snv
|
|
2.9E-02
|
Impaired cognition
|
Mental Disorders
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs157580
|
0.882 |
0.160 |
19 |
44892009 |
intron variant |
G/A
|
snv
|
|
0.69
|
Chronic Kidney Diseases
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs157580
|
0.882 |
0.160 |
19 |
44892009 |
intron variant |
G/A
|
snv
|
|
0.69
|
Sleep Apnea, Obstructive
|
Respiratory Tract Diseases; Nervous System Diseases
|
0.010 |
1.000 |
1 |
2008 |
2008 |
rs157580
|
0.882 |
0.160 |
19 |
44892009 |
intron variant |
G/A
|
snv
|
|
0.69
|
Herpes Simplex Infections
|
Infections; Skin and Connective Tissue Diseases
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs157581
|
0.925 |
0.080 |
19 |
44892457 |
synonymous variant |
T/C
|
snv
|
0.25
|
0.29
|
Alzheimer's Disease
|
Nervous System Diseases; Mental Disorders
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs157581
|
0.925 |
0.080 |
19 |
44892457 |
synonymous variant |
T/C
|
snv
|
0.25
|
0.29
|
Mild cognitive disorder
|
Mental Disorders
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs157582
|
0.851 |
0.160 |
19 |
44892962 |
intron variant |
C/T
|
snv
|
0.24
|
0.29
|
Mental deterioration
|
Mental Disorders
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs157582
|
0.851 |
0.160 |
19 |
44892962 |
intron variant |
C/T
|
snv
|
0.24
|
0.29
|
Impaired cognition
|
Mental Disorders
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs157590
|
0.882 |
0.160 |
19 |
44895459 |
intron variant |
A/C
|
snv
|
|
0.60
|
Behavioral variant of frontotemporal dementia
|
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs157590
|
0.882 |
0.160 |
19 |
44895459 |
intron variant |
A/C
|
snv
|
|
0.60
|
Primary Progressive Aphasia (disorder)
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs2075650
|
0.662 |
0.360 |
19 |
44892362 |
intron variant |
A/G
|
snv
|
0.13
|
0.13
|
Mild cognitive disorder
|
Mental Disorders
|
0.010 |
1.000 |
1 |
2018 |
2018 |
rs2075650
|
0.662 |
0.360 |
19 |
44892362 |
intron variant |
A/G
|
snv
|
0.13
|
0.13
|
Depressive disorder
|
Mental Disorders
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs2075650
|
0.662 |
0.360 |
19 |
44892362 |
intron variant |
A/G
|
snv
|
0.13
|
0.13
|
Primary Progressive Aphasia (disorder)
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs2075650
|
0.662 |
0.360 |
19 |
44892362 |
intron variant |
A/G
|
snv
|
0.13
|
0.13
|
Behavioral variant of frontotemporal dementia
|
Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs2075650
|
0.662 |
0.360 |
19 |
44892362 |
intron variant |
A/G
|
snv
|
0.13
|
0.13
|
Endometrial Carcinoma
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications
|
0.010 |
1.000 |
1 |
2016 |
2016 |
rs2075650
|
0.662 |
0.360 |
19 |
44892362 |
intron variant |
A/G
|
snv
|
0.13
|
0.13
|
Hypertriglyceridemia
|
Nutritional and Metabolic Diseases
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs2075650
|
0.662 |
0.360 |
19 |
44892362 |
intron variant |
A/G
|
snv
|
0.13
|
0.13
|
Carotid Artery Diseases
|
Nervous System Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2009 |
2009 |