rs1114167294, FOXP4

N. diseases: 4
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.
Feeding difficulties
CUI: C0232466
Disease: Feeding difficulties
62 0.925 6 41587455 frameshift variant T/- del 0.700 0
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
553 0.925 6 41587455 frameshift variant T/- del 0.700 0
Laryngeal hypoplasia
CUI: C0431527
Disease: Laryngeal hypoplasia
2 0.925 6 41587455 frameshift variant T/- del 0.700 0
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
87 0.925 6 41587455 frameshift variant T/- del 0.700 0