CASZ1, castor zinc finger 1, 54897

N. diseases: 132; N. variants: 15
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: rs17035646
rs17035646 		1 10736490 intron variant G/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 3 2018 2019
dbSNP: rs10157038
rs10157038 		1 10652408 non coding transcript exon variant C/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs12046278
rs12046278 		1 10739520 intron variant T/C snv 0.36
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs12046278
rs12046278 		1 10739520 intron variant T/C snv 0.36
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs12046278
rs12046278 		1 10739520 intron variant T/C snv 0.36
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs17035646
rs17035646 		1 10736490 intron variant G/A;T snv
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17035646
rs17035646 		1 10736490 intron variant G/A;T snv
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17035646
rs17035646 		1 10736490 intron variant G/A;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs17035646
rs17035646 		1 10736490 intron variant G/A;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs17035646
rs17035646 		1 10736490 intron variant G/A;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs284262
rs284262 		1 10683306 intron variant T/C snv 0.57
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs284316
rs284316 		1 10673024 intron variant T/C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs284316
rs284316 		1 10673024 intron variant T/C;G snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs34071855
rs34071855 		1 10738432 intron variant C/G;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs34071855
rs34071855 		1 10738432 intron variant C/G;T snv
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2019 2019
dbSNP: rs34071855
rs34071855 		1 10738432 intron variant C/G;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs34071855
rs34071855 		1 10738432 intron variant C/G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs35295665
rs35295665 		1 10737371 intron variant -/C delins
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs35295665
rs35295665 		1 10737371 intron variant -/C delins
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs544722
rs544722 		1 10682985 intron variant T/C snv 0.57
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs74748843
rs74748843 		1 10670853 intron variant C/T snv 2.2E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs11121615
rs11121615 		1.000 0.040 1 10765520 intron variant C/T snv 0.49
CUI: C0042345
Disease: Varicosity
Varicosity 		Cardiovascular Diseases 0.710 1.000 3 2018 2019
dbSNP: rs11121615
rs11121615 		1.000 0.040 1 10765520 intron variant C/T snv 0.49
CUI: C0235522
Disease: Disorder of vein
Disorder of vein 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs59985166
rs59985166 		1.000 0.040 1 10662447 intron variant C/T snv 4.9E-02
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs59985166
rs59985166 		1.000 0.040 1 10662447 intron variant C/T snv 4.9E-02
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.700 1.000 1 2019 2019