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: rs1136905
rs1136905 		0.882 0.120 6 32518660 missense variant T/A;C snv 4.2E-03
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1136905
rs1136905 		0.882 0.120 6 32518660 missense variant T/A;C snv 4.2E-03
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1136905
rs1136905 		0.882 0.120 6 32518660 missense variant T/A;C snv 4.2E-03
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs112209031
rs112209031 		1.000 0.040 6 32524630 intron variant T/C;G snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs112209031
rs112209031 		1.000 0.040 6 32524630 intron variant T/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs113397282
rs113397282 		1.000 0.040 6 32520273 intron variant T/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs113397282
rs113397282 		1.000 0.040 6 32520273 intron variant T/C;G snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs114604222
rs114604222 		6 32517846 intron variant A/G snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs114812317
rs114812317 		1.000 0.040 6 32531497 upstream gene variant G/A snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs114812317
rs114812317 		1.000 0.040 6 32531497 upstream gene variant G/A snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs114875775
rs114875775 		1.000 0.040 6 32521255 intron variant A/T snv 1.8E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs114875775
rs114875775 		1.000 0.040 6 32521255 intron variant A/T snv 1.8E-02
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs115641444
rs115641444 		1.000 0.040 6 32517285 downstream gene variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs115641444
rs115641444 		1.000 0.040 6 32517285 downstream gene variant C/G;T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs117616320
rs117616320 		1.000 0.040 6 32526927 intron variant C/A snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs117616320
rs117616320 		1.000 0.040 6 32526927 intron variant C/A snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs139480376
rs139480376 		1.000 0.040 6 32522469 intron variant A/C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs139480376
rs139480376 		1.000 0.040 6 32522469 intron variant A/C snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs139547629
rs139547629 		1.000 0.040 6 32518167 intron variant T/G snv 1.1E-04
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs139547629
rs139547629 		1.000 0.040 6 32518167 intron variant T/G snv 1.1E-04
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs140849564
rs140849564 		1.000 0.040 6 32522830 intron variant A/G snv 3.6E-02
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs140849564
rs140849564 		1.000 0.040 6 32522830 intron variant A/G snv 3.6E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs144532965
rs144532965 		1.000 0.040 6 32522018 missense variant T/A;C;G snv 1.1E-02; 4.0E-02; 1.2E-04
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs144532965
rs144532965 		1.000 0.040 6 32522018 missense variant T/A;C;G snv 1.1E-02; 4.0E-02; 1.2E-04
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs145470632
rs145470632 		1.000 0.040 6 32525469 intron variant A/G snv 2.8E-03
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017