ZNF318, zinc finger protein 318, 24149

N. diseases: 20; N. variants: 9
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: rs10948071
rs10948071 		6 43312975 intron variant C/T snv 0.46
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 3 2017 2018
dbSNP: rs1563788
rs1563788 		6 43340625 intron variant C/T snv 0.42
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 3 2015 2018
dbSNP: rs10948071
rs10948071 		6 43312975 intron variant C/T snv 0.46
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2018 2018
dbSNP: rs9394948
rs9394948 		6 43367017 intron variant A/C;G snv
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 2 2018 2019
dbSNP: rs10948071
rs10948071 		6 43312975 intron variant C/T snv 0.46
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs10948071
rs10948071 		6 43312975 intron variant C/T snv 0.46
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs145629243
rs145629243 		6 43339661 missense variant G/A snv 6.7E-03 7.4E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1563788
rs1563788 		6 43340625 intron variant C/T snv 0.42
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs1563788
rs1563788 		6 43340625 intron variant C/T snv 0.42
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1563788
rs1563788 		6 43340625 intron variant C/T snv 0.42
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2254303
rs2254303 		6 43308652 non coding transcript exon variant G/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6930689
rs6930689 		6 43325892 intron variant T/C snv 0.42
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs73416724
rs73416724 		1.000 0.040 6 43370064 non coding transcript exon variant A/G snv 0.11
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs73416724
rs73416724 		1.000 0.040 6 43370064 non coding transcript exon variant A/G snv 0.11
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs77915916
rs77915916 		6 43319984 intron variant A/T snv 5.9E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs77915916
rs77915916 		6 43319984 intron variant A/T snv 5.9E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs141660717
rs141660717 		1.000 0.080 6 43354899 missense variant T/C snv 7.2E-05 3.6E-04
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.700 0