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: rs11613352
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 4 2010 2018
dbSNP: rs11613352
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 4 2010 2018
dbSNP: rs11613352
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018