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: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2008 2018
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2009 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 1 2011 2019
dbSNP: rs8103315
rs8103315
1.000 0.080 19 44750911 intron variant C/A snv 9.1E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.800 1.000 1 2011 2018
dbSNP: rs10401176
rs10401176
1.000 0.080 19 44750234 intron variant C/G;T snv 0.17
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 2 2018 2019
dbSNP: rs2965169
rs2965169
0.925 0.120 19 44747899 non coding transcript exon variant A/C snv 0.50
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 2 2018 2019
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2016 2018
dbSNP: rs10401176
rs10401176
1.000 0.080 19 44750234 intron variant C/G;T snv 0.17
High density lipoprotein measurement
0.700 1.000 1 2019 2019
dbSNP: rs114036675
rs114036675
1.000 0.080 19 44759439 missense variant G/A snv 2.4E-03 5.1E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2019 2019
dbSNP: rs12459810
rs12459810
1.000 0.080 19 44746404 upstream gene variant C/T snv 0.21
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2018 2018
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0011847
Disease: Diabetes
Diabetes
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
0.700 1.000 1 2009 2009
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
High density lipoprotein measurement
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2016 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0018801
Disease: Heart failure
Heart failure
0.700 1.000 1 2016 2016