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: 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: 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: rs880315
rs880315
0.925 0.120 1 10736809 intron variant T/C snv 0.32
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs880315
rs880315
0.925 0.120 1 10736809 intron variant T/C snv 0.32
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
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: rs199867187
rs199867187
1.000 0.080 1 10637822 3 prime UTR variant AA/-;A;AAA;AAAA delins 0.29
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs59304342
rs59304342
1.000 0.080 1 10693037 intron variant T/A snv 5.0E-02
CUI: C0002170
Disease: Alopecia
Alopecia
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs880315
rs880315
0.925 0.120 1 10736809 intron variant T/C snv 0.32
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011