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: rs387906943
rs387906943
1.000 0.160 1 43736300 missense variant C/A snv
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.800 1.000 1 2011 2011
dbSNP: rs6674176
rs6674176
1 43914285 3 prime UTR variant G/A snv 0.64
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2017 2019
dbSNP: rs11210927
rs11210927
1 43800749 intron variant A/G snv 0.35
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs112984125
rs112984125
1.000 0.040 1 43707752 intron variant G/A snv 0.25
Attention deficit hyperactivity disorder
Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs11577684
rs11577684
1 43788609 intron variant C/G snv 0.27
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs12040333
rs12040333
1.000 0.080 1 43848369 intron variant G/A;C snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
Nutritional and Metabolic Diseases; Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs12040333
rs12040333
1.000 0.080 1 43848369 intron variant G/A;C snv
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs12122504
rs12122504
1 43791148 intron variant C/G snv 0.36
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12133508
rs12133508
1 43812074 intron variant C/T snv 0.39
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs12410444
rs12410444
1.000 0.040 1 43723048 intron variant A/G snv 0.25
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs12410444
rs12410444
1.000 0.040 1 43723048 intron variant A/G snv 0.25
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs246776
rs246776
1 43809028 intron variant C/T snv 0.45
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2486012
rs2486012
1 43907737 intron variant A/G snv 9.3E-02
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2906455
rs2906455
1 43876223 intron variant T/C snv 0.91
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs3011225
rs3011225
1.000 0.080 1 43853701 intron variant G/A snv 0.60
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
Nutritional and Metabolic Diseases; Nervous System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs4660261
rs4660261
1 43763926 intron variant G/A snv 0.69
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4660749
rs4660749
1 43784630 intron variant T/G snv 0.90
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs56319043
rs56319043
0.925 0.040 1 43705540 intron variant C/T snv 0.17
CUI: C3160814
Disease: Cannabis use
Cannabis use
0.700 1.000 1 2019 2019
dbSNP: rs56319043
rs56319043
0.925 0.040 1 43705540 intron variant C/T snv 0.17
Attention deficit hyperactivity disorder
Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs6429637
rs6429637
1 43732860 intron variant A/G snv 0.33
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs6656457
rs6656457
1 43767991 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs6701645
rs6701645
1 43788843 intron variant C/G;T snv
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2012 2012
dbSNP: rs1557612719
rs1557612719
1.000 0.160 1 43930201 stop lost G/T snv
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 12
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0