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: rs673548
rs673548
0.925 0.120 2 21014672 intron variant G/A;T snv
High density lipoprotein measurement
0.800 1.000 2 2012 2019
dbSNP: rs673548
rs673548
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2009 2019
dbSNP: rs673548
rs673548
0.925 0.120 2 21014672 intron variant G/A;T snv
Low density lipoprotein cholesterol measurement
0.800 1.000 1 2012 2018
dbSNP: rs673548
rs673548
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.800 1.000 1 2012 2012
dbSNP: rs673548
rs673548
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2012 2018
dbSNP: rs673548
rs673548
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2012 2012
dbSNP: rs673548
rs673548
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 1 2012 2012
dbSNP: rs673548
rs673548
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.700 1.000 1 2009 2009
dbSNP: rs673548
rs673548
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1.000 1 2009 2009
dbSNP: rs673548
rs673548
0.925 0.120 2 21014672 intron variant G/A;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012