rs104894290, RAG2;RAG1

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.
Omenn Syndrome
CUI: C2700553
Disease: Omenn Syndrome
48 1.000 0.120 11 36576039 missense variant A/G snv 0.800 1.000 6 1998 2011