rs966888627, 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 48797660 splice donor variant C/A;G;T snv 4.0E-06; 8.0E-06 0.700 0