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: rs28499105
rs28499105
ARL15
5 53978637 intron variant G/A snv 0.67
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs35006
rs35006
ARL15
1.000 0.040 5 54146895 intron variant C/G snv 0.24
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs35951
rs35951
ARL15
1.000 0.080 5 54296531 intron variant G/T snv 0.73
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		0.700 1.000 1 2014 2014
dbSNP: rs35951
rs35951
ARL15
1.000 0.080 5 54296531 intron variant G/T snv 0.73
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.700 1.000 1 2014 2014
dbSNP: rs35951
rs35951
ARL15
1.000 0.080 5 54296531 intron variant G/T snv 0.73
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		0.700 1.000 1 2014 2014
dbSNP: rs3776712
rs3776712
ARL15
5 54008349 intron variant T/C snv 0.28
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs4865796
rs4865796
ARL15
1.000 0.080 5 53976834 intron variant G/A snv 0.72
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2018 2018
dbSNP: rs4865796
rs4865796
ARL15
1.000 0.080 5 53976834 intron variant G/A snv 0.72
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs4865796
rs4865796
ARL15
1.000 0.080 5 53976834 intron variant G/A snv 0.72
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs6450176
rs6450176
ARL15
5 54002195 intron variant G/A snv 0.27
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs702634
rs702634
ARL15
1.000 0.080 5 53975590 intron variant G/A snv 0.72
CUI: C0001925
Disease: Albuminuria
Albuminuria 		0.700 1.000 1 2018 2018
dbSNP: rs702634
rs702634
ARL15
1.000 0.080 5 53975590 intron variant G/A snv 0.72
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs7719168
rs7719168
ARL15
5 53996560 intron variant A/C snv 8.7E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs7735249
rs7735249
ARL15
5 54014309 intron variant C/G snv 9.0E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2016 2016
dbSNP: rs7735249
rs7735249
ARL15
5 54014309 intron variant C/G snv 9.0E-02
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs79760705
rs79760705
ARL15
5 54002886 intron variant G/T snv 8.5E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019