SLC22A3, solute carrier family 22 member 3, 6581

N. diseases: 154; N. variants: 30
Disease: Coronary heart disease ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2048327
rs2048327 		0.851 0.120 6 160442500 intron variant T/C snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 2 2009 2014
dbSNP: rs3088442
rs3088442 		0.827 0.120 6 160451620 3 prime UTR variant G/A snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015