rs74315378, 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 168291213 missense variant T/G snv 0.710 1.000 1 2007 2007