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: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2012 2012
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2016 2019
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0018801
Disease: Heart failure
Heart failure 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0011847
Disease: Diabetes
Diabetes 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1728918
rs1728918 		0.827 0.160 2 27412596 upstream gene variant A/G;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2016 2016