Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs13107325
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 11 2010 2019
dbSNP: rs13107325
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2010 2018
dbSNP: rs13107325
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 8 2011 2019
dbSNP: rs13107325
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 7 2011 2019
dbSNP: rs13107325
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 3 2011 2018
dbSNP: rs13107325
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.800 1.000 1 2011 2011
dbSNP: rs13135092
rs13135092
SLC39A8
4 102276925 intron variant A/G snv 5.1E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 3 2015 2019
dbSNP: rs13107325
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.750 1.000 2 2015 2019
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2016 2018
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0011847
Disease: Diabetes
Diabetes 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0018801
Disease: Heart failure
Heart failure 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2016 2016
dbSNP: rs13114738
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs13107325
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017