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: rs1077835
rs1077835
15 58431227 intron variant A/G snv 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 5 2015 2019
dbSNP: rs1077835
rs1077835
15 58431227 intron variant A/G snv 0.34
High density lipoprotein measurement
0.800 1.000 3 2013 2019
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2012 2018
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
High density lipoprotein measurement
0.800 1.000 2 2012 2018
dbSNP: rs1077835
rs1077835
15 58431227 intron variant A/G snv 0.34
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs11631342
rs11631342
1.000 0.040 15 58432184 non coding transcript exon variant A/G snv 5.6E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.700 1.000 1 2018 2018
dbSNP: rs12148780
rs12148780
1.000 0.080 15 58289090 intron variant A/G snv 0.14
High density lipoprotein measurement
0.700 1.000 1 2019 2019
dbSNP: rs12148780
rs12148780
1.000 0.080 15 58289090 intron variant A/G snv 0.14
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.700 1.000 1 2019 2019
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2012 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0018801
Disease: Heart failure
Heart failure
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0011847
Disease: Diabetes
Diabetes
0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs6494005
rs6494005
1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.700 1.000 1 2018 2018
dbSNP: rs6494005
rs6494005
1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2012 2017