rs911707459, PIBF1

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 cerebral hernia
CUI: C0014065
Disease: Congenital cerebral hernia
6 0.925 0.120 13 72965358 missense variant A/T snv 7.0E-06 0.700 0
JOUBERT SYNDROME 33
CUI: C4540389
Disease: JOUBERT SYNDROME 33
5 0.925 0.120 13 72965358 missense variant A/T snv 7.0E-06 0.700 0