Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1557136818
rs1557136818
MECP2
0.925 0.120 X 154031259 missense variant C/T snv
CUI: C1843367
Disease: Poor school performance
Poor school performance 		0.700 0
dbSNP: rs1557136818
rs1557136818
MECP2
0.925 0.120 X 154031259 missense variant C/T snv
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		0.700 0
dbSNP: rs1557136818
rs1557136818
MECP2
0.925 0.120 X 154031259 missense variant C/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 0
dbSNP: rs1557136818
rs1557136818
MECP2
0.925 0.120 X 154031259 missense variant C/T snv
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		0.700 0