ZFHX3, zinc finger homeobox 3, 463

N. diseases: 85; N. variants: 39
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: rs12930834
rs12930834 		16 72917728 intron variant A/C snv 0.16
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs12932445
rs12932445 		0.925 0.080 16 73035989 intron variant T/C snv 0.18
CUI: C1531624
Disease: Cardioembolic stroke
Cardioembolic stroke 		0.700 1.000 1 2018 2018
dbSNP: rs12932445
rs12932445 		0.925 0.080 16 73035989 intron variant T/C snv 0.18
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs16972552
rs16972552 		16 73776555 intron variant C/G;T snv
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1858800
rs1858800 		1.000 0.120 16 72990377 intron variant C/T snv 0.28
CUI: C0848558
Disease: Hypospadias
Hypospadias 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2229288
rs2229288 		16 72794405 missense variant C/A snv 2.5E-03 2.1E-03
CUI: C0029445
Disease: Bone necrosis
Bone necrosis 		Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases 0.700 1.000 1 2015 2015
dbSNP: rs328317
rs328317 		1.000 0.040 16 73809907 intron variant A/G snv 7.4E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs328384
rs328384 		1.000 0.040 16 73805897 intron variant G/A snv 0.40
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs328389
rs328389 		1.000 0.040 16 73804268 intron variant G/A snv 0.16
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs328395
rs328395 		1.000 0.040 16 73801800 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs328398
rs328398 		1.000 0.040 16 73801272 intron variant A/G snv 5.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs34516333
rs34516333 		16 73114768 intron variant G/T snv 0.17
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs417278
rs417278 		16 73796577 intron variant T/C snv 0.43
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4404097
rs4404097 		1.000 0.080 16 72998133 intron variant G/A snv 0.13
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4499262
rs4499262 		1.000 0.080 16 73025260 intron variant C/A;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs4788694
rs4788694 		16 73036184 intron variant C/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs62051555
rs62051555 		16 72796640 missense variant C/A;G snv 4.0E-06; 2.6E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs62055084
rs62055084 		16 73063946 intron variant C/T snv 0.19
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs6564524
rs6564524 		16 73761105 intron variant C/T snv 0.24
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7189864
rs7189864 		1.000 0.040 16 73600037 intron variant G/C snv 0.43
CUI: C1863416
Disease: Autosomal dominant compelling helio ophthalmic outburst syndrome
Autosomal dominant compelling helio ophthalmic outburst syndrome 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2016 2016
dbSNP: rs7190256
rs7190256 		0.851 0.120 16 72963084 intron variant C/T snv 0.94
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs7190256
rs7190256 		0.851 0.120 16 72963084 intron variant C/T snv 0.94
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs7190256
rs7190256 		0.851 0.120 16 72963084 intron variant C/T snv 0.94
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs7190256
rs7190256 		0.851 0.120 16 72963084 intron variant C/T snv 0.94
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7190256
rs7190256 		0.851 0.120 16 72963084 intron variant C/T snv 0.94
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2016 2016