rs192669225, AMPD2

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 anomaly of brain
CUI: C0266449
Disease: Congenital anomaly of brain
7 0.925 0.040 1 109628692 missense variant G/A snv 0.700 0
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.925 0.040 1 109628692 missense variant G/A snv 0.700 0
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
553 0.925 0.040 1 109628692 missense variant G/A snv 0.700 0