rs267606826, FOXG1

N. diseases: 38
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.
Oculomotor apraxia
CUI: C3489733
Disease: Oculomotor apraxia
14 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Partial or complete agenesis of corpus callosum
CUI: C1857278
Disease: Partial or complete agenesis of corpus callosum
6 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Pediatric failure to thrive
CUI: C2315100
Disease: Pediatric failure to thrive
122 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Poor school performance
CUI: C1843367
Disease: Poor school performance
411 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Proportionate short stature
CUI: C0878660
Disease: Proportionate short stature
11 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Protruding ear
CUI: C1855285
Disease: Protruding ear
6 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Recurrent urinary tract infection
CUI: C0262655
Disease: Recurrent urinary tract infection
21 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Secondary microcephaly
CUI: C0431352
Disease: Secondary microcephaly
20 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Short stature
CUI: C0349588
Disease: Short stature
292 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Sleep disturbances
CUI: C0037317
Disease: Sleep disturbances
74 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Stereotypic Movement Disorder
CUI: C0038273
Disease: Stereotypic Movement Disorder
26 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Strabismus
CUI: C0038379
Disease: Strabismus
89 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0
Weight less than 3rd percentile
CUI: C1844806
Disease: Weight less than 3rd percentile
27 0.708 0.520 14 28767903 stop gained C/A;G;T snv 0.700 0