SLIT3, slit guidance ligand 3, 6586

N. diseases: 62; N. variants: 7
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: rs4282339
rs4282339 		5 168829235 intron variant G/A snv 0.18
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 4 2010 2019
dbSNP: rs2974438
rs2974438 		5 168823898 intron variant G/A snv 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2014 2019
dbSNP: rs12188351
rs12188351 		0.925 0.120 5 168959084 intron variant G/A snv 3.8E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs12188351
rs12188351 		0.925 0.120 5 168959084 intron variant G/A snv 3.8E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015
dbSNP: rs4282339
rs4282339 		5 168829235 intron variant G/A snv 0.18
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs76493495
rs76493495 		5 169092117 intron variant G/A snv 2.8E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs7735612
rs7735612 		1.000 0.040 5 169082727 intron variant T/C snv 0.33
CUI: C2063866
Disease: Depressive Disorder, Treatment-Resistant
Depressive Disorder, Treatment-Resistant 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.040 1.000 4 2010 2017
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.040 0.750 4 2014 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.040 0.750 4 2014 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.030 0.667 3 2012 2014
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.030 1.000 3 2010 2017
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.030 1.000 3 2010 2017
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2014 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C1512409
Disease: Hepatocarcinogenesis
Hepatocarcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C4086165
Disease: Childhood Neuroblastoma
Childhood Neuroblastoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs11134527
rs11134527 		0.677 0.400 5 168768351 intron variant G/A snv 0.25
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
Cervical Intraepithelial Neoplasia 		Neoplasms 0.010 1.000 1 2017 2017