rs1352056360, LCAT

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.
Cholesteryl Ester Transfer Protein Deficiency
CUI: C0342883
Disease: Cholesteryl Ester Transfer Protein Deficiency
5 0.925 0.080 16 67940467 missense variant C/G snv 1.2E-05 0.010 1.000 1 1998 1998
Hdl Deficiency, Type 2
CUI: C3711531
Disease: Hdl Deficiency, Type 2
1 0.925 0.080 16 67940467 missense variant C/G snv 1.2E-05 0.010 1.000 1 1998 1998