rs775394591, FREM2

N. diseases: 5
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.
Abnormality of cardiovascular system morphology
CUI: C4049796
Disease: Abnormality of cardiovascular system morphology
13 0.851 0.120 13 38784727 inframe deletion TCT/- delins 2.8E-05 0.700 0
Congenital diaphragmatic hernia
CUI: C0235833
Disease: Congenital diaphragmatic hernia
31 0.851 0.120 13 38784727 inframe deletion TCT/- delins 2.8E-05 0.700 0
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
553 0.851 0.120 13 38784727 inframe deletion TCT/- delins 2.8E-05 0.700 0
Microcephaly (physical finding)
CUI: C4551563
Disease: Microcephaly (physical finding)
246 0.851 0.120 13 38784727 inframe deletion TCT/- delins 2.8E-05 0.700 0
Patent ductus arteriosus
CUI: C0013274
Disease: Patent ductus arteriosus
56 0.851 0.120 13 38784727 inframe deletion TCT/- delins 2.8E-05 0.700 0