SNAP25, synaptosome associated protein 25, 6616

N. diseases: 283; N. variants: 15
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: rs363050
rs363050
0.790 0.240 20 10253609 intron variant G/A snv 0.57
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs363050
rs363050
0.790 0.240 20 10253609 intron variant G/A snv 0.57
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs363050
rs363050
0.790 0.240 20 10253609 intron variant G/A snv 0.57
CUI: C4551584
Disease: Brain atrophy
Brain atrophy
Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs363050
rs363050
0.790 0.240 20 10253609 intron variant G/A snv 0.57
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs363050
rs363050
0.790 0.240 20 10253609 intron variant G/A snv 0.57
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs3746544
rs3746544
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs3746544
rs3746544
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3746544
rs3746544
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs3746544
rs3746544
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68
CUI: C0424101
Disease: Inattention
Inattention
0.010 1.000 1 2017 2017
dbSNP: rs3746544
rs3746544
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3746544
rs3746544
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3746544
rs3746544
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
Behavior and Behavior Mechanisms 0.010 1.000 1 2017 2017
dbSNP: rs3746544
rs3746544
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs3787283
rs3787283
0.882 0.040 20 10303770 intron variant A/G snv 0.34
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs3787283
rs3787283
0.882 0.040 20 10303770 intron variant A/G snv 0.34
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs6039769
rs6039769
1.000 0.040 20 10218306 intron variant A/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2020 2020
dbSNP: rs6108461
rs6108461
1.000 0.040 20 10286622 intron variant A/G snv 0.57
Attention deficit hyperactivity disorder
Mental Disorders 0.010 1.000 1 2017 2017