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: rs145470632
rs145470632
1.000 0.040 6 32525469 intron variant A/G snv 2.8E-03
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs147793969
rs147793969
1.000 0.040 6 32526115 intron variant C/T snv 0.16
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs147793969
rs147793969
1.000 0.040 6 32526115 intron variant C/T snv 0.16
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs149961934
rs149961934
1.000 0.040 6 32520992 intron variant G/C snv
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs149961934
rs149961934
1.000 0.040 6 32520992 intron variant G/C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs184538485
rs184538485
1.000 0.040 6 32522589 intron variant A/C snv 4.8E-03
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs184538485
rs184538485
1.000 0.040 6 32522589 intron variant A/C snv 4.8E-03
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs184981897
rs184981897
1.000 0.040 6 32519189 intron variant C/A snv 1.8E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs184981897
rs184981897
1.000 0.040 6 32519189 intron variant C/A snv 1.8E-02
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs189600472
rs189600472
1.000 0.040 6 32526320 intron variant T/G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs189600472
rs189600472
1.000 0.040 6 32526320 intron variant T/G snv
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs191018606
rs191018606
6 32520304 intron variant T/A;C snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs191269336
rs191269336
1.000 0.040 6 32521819 intron variant A/T snv 0.20
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs191269336
rs191269336
1.000 0.040 6 32521819 intron variant A/T snv 0.20
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs191843781
rs191843781
1.000 0.040 6 32525190 intron variant T/C;G snv
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs191843781
rs191843781
1.000 0.040 6 32525190 intron variant T/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs193267147
rs193267147
1.000 0.040 6 32528783 intron variant G/A snv
Child Development Disorders, Pervasive
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs193267147
rs193267147
1.000 0.040 6 32528783 intron variant G/A snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs41553512
rs41553512
1.000 0.040 6 32518625 missense variant C/T snv 0.12 4.6E-02
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.700 1.000 1 2017 2017
dbSNP: rs72508457
rs72508457
1.000 0.080 6 32528394 intron variant C/A;G snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019