CTNNA3, catenin alpha 3, 29119

N. diseases: 73; N. variants: 33
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: rs2441727
rs2441727
10 66465128 intron variant A/G snv 0.21
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial
Respiratory Tract Diseases 0.800 1.000 1 2013 2013
dbSNP: rs587777134
rs587777134
1.000 10 67606868 missense variant A/T snv
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 13
0.800 1.000 1 2013 2013
dbSNP: rs72791417
rs72791417
1.000 0.080 10 65983896 intron variant A/T snv 0.11
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases 0.800 1.000 1 2013 2013
dbSNP: rs12764057
rs12764057
1.000 0.040 10 67085957 intron variant T/G snv 0.35
CUI: C0270736
Disease: Essential Tremor
Essential Tremor
Nervous System Diseases 0.720 0.667 3 2016 2018
dbSNP: rs7902091
rs7902091
1.000 0.040 10 66838534 intron variant C/A snv 0.29
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.710 1.000 1 2014 2014
dbSNP: rs7902091
rs7902091
1.000 0.040 10 66838534 intron variant C/A snv 0.29
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections
Infections 0.710 1.000 1 2014 2014
dbSNP: rs10762080
rs10762080
1.000 0.040 10 66637687 intron variant A/G snv 0.67
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs10822745
rs10822745
10 66194307 intron variant T/C snv 0.37
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs10823051
rs10823051
1.000 0.080 10 67504839 intron variant G/C snv 0.13
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs12356475
rs12356475
1.000 0.080 10 66001962 intron variant T/C snv 0.15
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic
Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.700 1.000 1 2015 2015
dbSNP: rs12773625
rs12773625
1.000 0.040 10 66919791 intron variant T/A snv 0.41
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs12773625
rs12773625
1.000 0.040 10 66919791 intron variant T/A snv 0.41
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1670140
rs1670140
0.925 0.040 10 65948601 intron variant T/C;G snv
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs1670140
rs1670140
0.925 0.040 10 65948601 intron variant T/C;G snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4745925
rs4745925
0.925 0.040 10 67051026 intron variant G/A;C snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4745925
rs4745925
0.925 0.040 10 67051026 intron variant G/A;C snv
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs4746582
rs4746582
10 66417570 intron variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs4746675
rs4746675
1.000 0.040 10 67192300 intron variant C/A snv 0.37
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2006 2006
dbSNP: rs533451950
rs533451950
10 67475334 intron variant T/C snv 1.4E-05
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs558363983
rs558363983
10 67453432 intron variant A/C;T snv 7.0E-06
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs560625443
rs560625443
10 67354852 intron variant G/A snv 5.6E-05
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs75495219
rs75495219
1.000 10 67151138 intron variant A/G snv 6.0E-02
Adverse effects, not elsewhere classified
0.700 1.000 1 2019 2019
dbSNP: rs7923367
rs7923367
0.925 0.040 10 67413145 intron variant G/A;C;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7923367
rs7923367
0.925 0.040 10 67413145 intron variant G/A;C;T snv
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs587777135
rs587777135
0.925 0.080 10 65966714 inframe deletion CAA/- delins
Arrhythmogenic Right Ventricular Dysplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.700 0