rs74315377, TBX19

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.
ACTH Deficiency, Isolated
CUI: C0271583
Disease: ACTH Deficiency, Isolated
11 1.000 0.120 1 168291339 missense variant C/T snv 4.0E-06 0.800 1.000 1 2001 2001