rs28934907, MECP2

N. diseases: 2
Source: BEFREE ×
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.
Rett Syndrome
CUI: C0035372
Disease: Rett Syndrome
54 0.732 0.320 X 154032268 missense variant G/A;C snv 0.840 1.000 4 1999 2017
Epilepsy
CUI: C0014544
Disease: Epilepsy
250 0.732 0.320 X 154032268 missense variant G/A;C snv 0.010 1.000 1 2010 2010