RELN, reelin, 5649

N. diseases: 178; N. variants: 52
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: rs10233848
rs10233848
7 103482198 non coding transcript exon variant A/G snv 0.42
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs11496125
rs11496125
7 103777110 intron variant C/T snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs12375196
rs12375196
7 103776094 intron variant C/A snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2041475
rs2041475
7 103547614 intron variant C/T snv 0.85
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs2965087
rs2965087
7 103471538 intron variant T/C snv 0.45
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms
Behavior and Behavior Mechanisms 0.010 1.000 1 2016 2016
dbSNP: rs6956101
rs6956101
7 103508155 intron variant A/G snv 0.17
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs78623212
rs78623212
7 103667180 intron variant C/T snv 1.5E-02
CUI: C2697766
Disease: Interleukin 18 Measurement
Interleukin 18 Measurement
0.700 1.000 1 2017 2017
dbSNP: rs7341475
rs7341475
0.851 0.240 7 103764368 intron variant G/A snv 0.17
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.860 0.857 7 2008 2019
dbSNP: rs7341475
rs7341475
0.851 0.240 7 103764368 intron variant G/A snv 0.17
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs7341475
rs7341475
0.851 0.240 7 103764368 intron variant G/A snv 0.17
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs7341475
rs7341475
0.851 0.240 7 103764368 intron variant G/A snv 0.17
Attention deficit hyperactivity disorder
Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs7341475
rs7341475
0.851 0.240 7 103764368 intron variant G/A snv 0.17
CUI: C0004936
Disease: Mental disorders
Mental disorders
Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs7341475
rs7341475
0.851 0.240 7 103764368 intron variant G/A snv 0.17
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
Behavior and Behavior Mechanisms 0.010 1.000 1 2017 2017
dbSNP: rs736707
rs736707
0.851 0.040 7 103489956 intron variant A/G snv 0.30
CUI: C0004936
Disease: Mental disorders
Mental disorders
Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs736707
rs736707
0.851 0.040 7 103489956 intron variant A/G snv 0.30
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs736707
rs736707
0.851 0.040 7 103489956 intron variant A/G snv 0.30
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs736707
rs736707
0.851 0.040 7 103489956 intron variant A/G snv 0.30
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
Behavior and Behavior Mechanisms 0.010 1.000 1 2017 2017
dbSNP: rs736707
rs736707
0.851 0.040 7 103489956 intron variant A/G snv 0.30
Attention deficit hyperactivity disorder
Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs736707
rs736707
0.851 0.040 7 103489956 intron variant A/G snv 0.30
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs362691
rs362691
0.882 0.120 7 103610714 missense variant G/A;C;T snv 1.2E-05; 0.12
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs362691
rs362691
0.882 0.120 7 103610714 missense variant G/A;C;T snv 1.2E-05; 0.12
CUI: C0162770
Disease: Right Ventricular Hypertrophy
Right Ventricular Hypertrophy
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs362691
rs362691
0.882 0.120 7 103610714 missense variant G/A;C;T snv 1.2E-05; 0.12
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs362719
rs362719
0.925 0.040 7 103545430 intron variant C/A snv 0.32
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.020 1.000 2 2010 2011
dbSNP: rs528528
rs528528
0.925 0.080 7 103748638 intron variant T/A;C snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.020 1.000 2 2015 2016
dbSNP: rs362719
rs362719
0.925 0.040 7 103545430 intron variant C/A snv 0.32
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2011 2011