rs1567886959, FOXN1

N. diseases: 3
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.
Congenital absence of thymus
CUI: C0685894
Disease: Congenital absence of thymus
2 0.882 0.160 17 28534814 frameshift variant C/- delins 0.700 0
Relative macrocephaly
CUI: C1849075
Disease: Relative macrocephaly
19 0.882 0.160 17 28534814 frameshift variant C/- delins 0.700 0
Severe T-cell immunodeficiency
CUI: C4025208
Disease: Severe T-cell immunodeficiency
2 0.882 0.160 17 28534814 frameshift variant C/- delins 0.700 0