WNT2B, Wnt family member 2B, 7482

N. diseases: 65; N. variants: 12
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: rs3790604
rs3790604 		1 112504257 intron variant C/A snv 7.8E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 3 2018 2019
dbSNP: rs10776752
rs10776752 		1 112501706 intron variant G/T snv 8.8E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2018 2018
dbSNP: rs10776752
rs10776752 		1 112501706 intron variant G/T snv 8.8E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2018 2019
dbSNP: rs3790604
rs3790604 		1 112504257 intron variant C/A snv 7.8E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 2 2018 2018
dbSNP: rs10776752
rs10776752 		1 112501706 intron variant G/T snv 8.8E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs10776752
rs10776752 		1 112501706 intron variant G/T snv 8.8E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1175646
rs1175646 		0.925 0.040 1 112465599 upstream gene variant G/A;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1175646
rs1175646 		0.925 0.040 1 112465599 upstream gene variant G/A;T snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs12037987
rs12037987 		1 112500200 intron variant T/C snv 8.6E-02
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs12037987
rs12037987 		1 112500200 intron variant T/C snv 8.6E-02
CUI: C0202194
Disease: Potassium measurement
Potassium measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1620668
rs1620668 		1 112481358 intron variant A/G snv 0.17
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs1620668
rs1620668 		1 112481358 intron variant A/G snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs2273368
rs2273368 		1 112521149 3 prime UTR variant C/G;T snv
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
dbSNP: rs351364
rs351364 		1 112502439 intron variant A/C;T snv 0.72
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs351364
rs351364 		1 112502439 intron variant A/C;T snv 0.72
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs351365
rs351365 		1.000 0.120 1 112503773 intron variant T/C;G snv
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs3790604
rs3790604 		1 112504257 intron variant C/A snv 7.8E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs3790604
rs3790604 		1 112504257 intron variant C/A snv 7.8E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs3790604
rs3790604 		1 112504257 intron variant C/A snv 7.8E-02
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs3790606
rs3790606 		1 112509564 intron variant G/C snv 0.26
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs6692731
rs6692731 		1 112476560 intron variant C/T snv 3.3E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7516521
rs7516521 		1 112512314 intron variant T/G snv 7.0E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7516521
rs7516521 		1 112512314 intron variant T/G snv 7.0E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs370244148
rs370244148 		0.882 0.160 1 112514896 stop gained C/A;T snv 1.6E-05; 1.2E-05
CUI: C0401151
Disease: Chronic diarrhea
Chronic diarrhea 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 0
dbSNP: rs370244148
rs370244148 		0.882 0.160 1 112514896 stop gained C/A;T snv 1.6E-05; 1.2E-05
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders 0.700 0