rs1554823375, WDR37

N. diseases: 8
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.
Cerebellar Hypoplasia
CUI: C0266470
Disease: Cerebellar Hypoplasia
26 0.851 0.160 10 1080454 missense variant C/T snv 0.700 0
Cerebellar vermis hypoplasia
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
26 0.851 0.160 10 1080454 missense variant C/T snv 0.700 0
Congenital ocular coloboma (disorder)
CUI: C0009363
Disease: Congenital ocular coloboma (disorder)
21 0.851 0.160 10 1080454 missense variant C/T snv 0.700 0
Developmental delay (disorder)
CUI: C0424605
Disease: Developmental delay (disorder)
68 0.851 0.160 10 1080454 missense variant C/T snv 0.700 0
Dilated ventricles (finding)
CUI: C3278923
Disease: Dilated ventricles (finding)
32 0.851 0.160 10 1080454 missense variant C/T snv 0.700 0
Dysmorphism
CUI: C1737329
Disease: Dysmorphism
16 0.851 0.160 10 1080454 missense variant C/T snv 0.700 0
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.851 0.160 10 1080454 missense variant C/T snv 0.700 0
Poor school performance
CUI: C1843367
Disease: Poor school performance
411 0.851 0.160 10 1080454 missense variant C/T snv 0.700 0