rs10790162, BUD13

N. diseases: 7
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 0.800 1.000 3 2011 2019
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 0.800 1.000 1 2011 2011
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 0.700 1.000 2 2011 2019
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 0.700 1.000 1 2012 2012
Hyper LDL cholesterolaemia
CUI: C2242712
Disease: Hyper LDL cholesterolaemia
19 0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 0.010 1.000 1 2017 2017
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 0.010 1.000 1 2017 2017
Hypochondroplasia (disorder)
CUI: C0410529
Disease: Hypochondroplasia (disorder)
42 0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 0.010 1.000 1 2014 2014