Source: ALL

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: rs9370867
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 < 0.001 1 2015 2015
dbSNP: rs9370867
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63
CUI: C0342882
Disease: Familial hypercholesterolemia - heterozygous
Familial hypercholesterolemia - heterozygous 		0.010 1.000 1 2014 2014
dbSNP: rs9370867
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		0.010 1.000 1 2012 2012
dbSNP: rs9370867
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63
CUI: C0745103
Disease: Hyperlipoproteinemia Type IIa
Hyperlipoproteinemia Type IIa 		0.010 1.000 1 2014 2014
dbSNP: rs9370867
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 < 0.001 1 2015 2015
dbSNP: rs9370867
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63
CUI: C0020445
Disease: Hypercholesterolemia, Familial
Hypercholesterolemia, Familial 		0.010 1.000 1 2014 2014
dbSNP: rs9370867
rs9370867
MYLIP
0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 < 0.001 1 2015 2015