rs1057519560, MYT1L

N. diseases: 2
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.
MENTAL RETARDATION, AUTOSOMAL DOMINANT 39
CUI: C4225296
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 39
8 1.000 2 1917264 missense variant A/G snv 0.700 0
Seizures
CUI: C0036572
Disease: Seizures
553 1.000 2 1917264 missense variant A/G snv 0.700 0