rs200879436, CEP152

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.
SECKEL SYNDROME 5
CUI: C3151187
Disease: SECKEL SYNDROME 5
6 1.000 15 48768237 missense variant T/C snv 1.0E-03 4.4E-03 0.700 1.000 1 2011 2011