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: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C1305855
Disease: Body mass index
Body mass index 		0.800 1.000 1 2012 2012
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 6 2015 2019
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.700 1.000 3 2012 2015
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2018 2019
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2018 2019
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2018 2019
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2012 2012
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0.700 1.000 1 2017 2017
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.700 1.000 1 2012 2012
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0.700 1.000 1 2017 2017
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C0202100
Disease: Insulin C-peptide measurement
Insulin C-peptide measurement 		0.700 1.000 1 2013 2013
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2012 2012
dbSNP: rs4841132
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2019 2019