SNX19, sorting nexin 19, 399979

N. diseases: 5; N. variants: 2
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: rs4459316
rs4459316 		11 130886281 intron variant T/C snv 0.44
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2298566
rs2298566 		0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs2298566
rs2298566 		0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs2298566
rs2298566 		0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs2298566
rs2298566 		0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs2298566
rs2298566 		0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2007 2007