rs749318884, LHX4

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.
Isolated somatotropin deficiency
CUI: C3714796
Disease: Isolated somatotropin deficiency
27 0.925 0.120 1 180248431 missense variant G/A snv 8.4E-05 3.5E-05 0.010 1.000 1 2012 2012
Pituitary dwarfism
CUI: C0013338
Disease: Pituitary dwarfism
12 0.925 0.120 1 180248431 missense variant G/A snv 8.4E-05 3.5E-05 0.010 1.000 1 2012 2012