rs104894023, LEP

N. diseases: 1
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.
LEPTIN DEFICIENCY OR DYSFUNCTION
CUI: C3554224
Disease: LEPTIN DEFICIENCY OR DYSFUNCTION
3 1.000 7 128254572 missense variant C/T snv 0.800 1.000 2 1998 2015