WNT3, Wnt family member 3, 7473

N. diseases: 140; N. variants: 22
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: rs199498
rs199498 		0.925 0.120 17 46788237 intron variant T/C;G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.800 1.000 1 2014 2014
dbSNP: rs199498
rs199498 		0.925 0.120 17 46788237 intron variant T/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs199506
rs199506 		17 46781665 intron variant A/C;G snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs199507
rs199507 		17 46781489 intron variant A/G;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs199512
rs199512 		17 46779986 intron variant T/A;C snv
CUI: C0023114
Disease: Handedness
Handedness 		0.700 1.000 1 2019 2019
dbSNP: rs199525
rs199525 		1.000 0.080 17 46770468 intron variant T/A;G snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs199525
rs199525 		1.000 0.080 17 46770468 intron variant T/A;G snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2018 2018
dbSNP: rs199525
rs199525 		1.000 0.080 17 46770468 intron variant T/A;G snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2018 2018
dbSNP: rs70600
rs70600 		1.000 0.080 17 46782655 intron variant C/G;T snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs786205887
rs786205887 		1.000 0.120 17 46773719 missense variant A/C;G snv
CUI: C1838703
Disease: Bladder Exstrophy and Epispadias Complex
Bladder Exstrophy and Epispadias Complex 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 0
dbSNP: rs1563304
rs1563304 		1.000 0.080 17 46797087 intron variant C/T snv 0.11
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs199528
rs199528 		17 46765770 intron variant C/T snv 0.13
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs916888
rs916888 		17 46785767 intron variant T/C snv 0.19
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2017 2019
dbSNP: rs916888
rs916888 		17 46785767 intron variant T/C snv 0.19
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2018 2018
dbSNP: rs916888
rs916888 		17 46785767 intron variant T/C snv 0.19
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2018 2018
dbSNP: rs916888
rs916888 		17 46785767 intron variant T/C snv 0.19
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs3809857
rs3809857 		1.000 17 46770948 intron variant G/T snv 0.25
CUI: C0810364
Disease: Cleft Lip with or without Cleft Palate
Cleft Lip with or without Cleft Palate 		0.010 1.000 1 2018 2018
dbSNP: rs2074404
rs2074404 		0.925 0.120 17 46788073 intron variant T/G snv 0.27
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.800 1.000 1 2010 2010
dbSNP: rs2074404
rs2074404 		0.925 0.120 17 46788073 intron variant T/G snv 0.27
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2074404
rs2074404 		0.925 0.120 17 46788073 intron variant T/G snv 0.27
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2074404
rs2074404 		0.925 0.120 17 46788073 intron variant T/G snv 0.27
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs199520
rs199520 		17 46776506 intron variant G/A snv 0.62
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs9890413
rs9890413 		1.000 17 46824083 intron variant G/A snv 0.63
CUI: C0810364
Disease: Cleft Lip with or without Cleft Palate
Cleft Lip with or without Cleft Palate 		0.010 1.000 1 2018 2018
dbSNP: rs199501
rs199501 		17 46785247 intron variant A/G snv 0.64
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs8069437
rs8069437 		17 46829583 intron variant T/C snv 0.82
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016