rs1557137745, MECP2

N. diseases: 2
Source: INFERRED ×
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.
Movement Disorders
CUI: C0026650
Disease: Movement Disorders
X 154032272 missense variant C/A snv 0.700 1.000 19 1993 2016
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
X 154032272 missense variant C/A snv 0.700 1.000 19 1993 2016