rs1350201776, ZNF335

N. diseases: 3
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.
Movement Disorders
CUI: C0026650
Disease: Movement Disorders
247 20 45952244 missense variant C/T snv 4.0E-06 0.700 1.000 5 2009 2016
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
350 20 45952244 missense variant C/T snv 4.0E-06 0.700 1.000 5 2009 2016
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
579 20 45952244 missense variant C/T snv 4.0E-06 0.700 1.000 5 2009 2016