rs1206736425, FCGR3B

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.
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
73 1 161626229 missense variant T/C snv 0.010 1.000 1 2018 2018
Developmental delay (disorder)
CUI: C0424605
Disease: Developmental delay (disorder)
68 1 161626229 missense variant T/C snv 0.010 1.000 1 2018 2018