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: rs1796518
rs1796518
6 26388444 intron variant C/T snv 0.32
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2019
dbSNP: rs1614887
rs1614887
6 26392793 synonymous variant G/A snv 0.53 0.63
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs1614887
rs1614887
6 26392793 synonymous variant G/A snv 0.53 0.63
CUI: C0021704
Disease: Intelligence
Intelligence
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2072803
rs2072803
1.000 0.040 6 26392287 missense variant G/C snv 8.6E-02 7.7E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs2072806
rs2072806
1.000 0.040 6 26384865 intron variant C/G snv 7.7E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs2072806
rs2072806
1.000 0.040 6 26384865 intron variant C/G snv 7.7E-02
CUI: C0018681
Disease: Headache
Headache
Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2018 2018
dbSNP: rs2237234
rs2237234
1.000 0.040 6 26391166 3 prime UTR variant G/A snv 0.24
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs2237234
rs2237234
1.000 0.040 6 26391166 3 prime UTR variant G/A snv 0.24
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs7756881
rs7756881
1.000 0.040 6 26389698 intron variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs9461249
rs9461249
1.000 0.040 6 26383158 5 prime UTR variant T/C snv 0.23
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2012 2012