rs1555696625, NFIX

N. diseases: 7
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.
Agenesis of corpus callosum
CUI: C0175754
Disease: Agenesis of corpus callosum
45 0.851 0.360 19 13025409 missense variant G/A snv 0.700 0
Blue sclera
CUI: C0542514
Disease: Blue sclera
13 0.851 0.360 19 13025409 missense variant G/A snv 0.700 0
Laryngomalacia
CUI: C0264303
Disease: Laryngomalacia
18 0.851 0.360 19 13025409 missense variant G/A snv 0.700 0
Marshall-Smith syndrome
CUI: C0265211
Disease: Marshall-Smith syndrome
17 0.851 0.360 19 13025409 missense variant G/A snv 0.700 0
Pediatric failure to thrive
CUI: C2315100
Disease: Pediatric failure to thrive
122 0.851 0.360 19 13025409 missense variant G/A snv 0.700 0
Poor school performance
CUI: C1843367
Disease: Poor school performance
411 0.851 0.360 19 13025409 missense variant G/A snv 0.700 0
Prominent forehead
CUI: C1837260
Disease: Prominent forehead
25 0.851 0.360 19 13025409 missense variant G/A snv 0.700 0