rs1569144348, TCF20

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.
Neurodevelopmental abnormality
CUI: C4022737
Disease: Neurodevelopmental abnormality
19 22 42210564 frameshift variant CT/- delins 0.700 0