Source: GWASDB

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: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2009 2019
dbSNP: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2009 2019
dbSNP: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 1 2012 2019
dbSNP: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 1.000 1 2011 2011
dbSNP: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2009 2009
dbSNP: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174570
rs174570
0.882 0.200 11 61829740 intron variant C/T snv 0.15
High density lipoprotein measurement
0.700 1.000 1 2012 2012