rs11206517, PCSK9

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hypochondroplasia (disorder)
CUI: C0410529
Disease: Hypochondroplasia (disorder)
42 1.000 0.120 1 55060755 intron variant T/C;G snv 0.010 1.000 1 2016 2016
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 1.000 0.120 1 55060755 intron variant T/C;G snv 0.010 1.000 1 2016 2016
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 1.000 0.120 1 55060755 intron variant T/C;G snv 0.700 1.000 1 2012 2012
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 1.000 0.120 1 55060755 intron variant T/C;G snv 0.700 1.000 1 2012 2012