rs2229738, CPT1A

N. diseases: 2
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.
Lipids measurement
CUI: C0523744
Disease: Lipids measurement
53 11 68794860 missense variant C/G;T snv 6.3E-02 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 11 68794860 missense variant C/G;T snv 6.3E-02 0.700 1.000 1 2012 2012