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.
Small for gestational age (disorder)
CUI: C0235991
Disease: Small for gestational age (disorder)
34 0.742 0.320 18 12337505 missense variant C/T snv 0.700 1.000 1 2010 2010
SPINOCEREBELLAR ATAXIA 28
CUI: C1853249
Disease: SPINOCEREBELLAR ATAXIA 28
11 0.742 0.320 18 12337505 missense variant C/T snv 0.800 1.000 7 2010 2017
Tinnitus
CUI: C0040264
Disease: Tinnitus
14 0.742 0.320 18 12337505 missense variant C/T snv 0.700 1.000 1 2010 2010
Vertigo
CUI: C0042571
Disease: Vertigo
35 0.742 0.320 18 12337505 missense variant C/T snv 0.700 1.000 1 2010 2010
Vitamin D Deficiency
CUI: C0042870
Disease: Vitamin D Deficiency
37 0.742 0.320 18 12337505 missense variant C/T snv 0.700 1.000 1 2010 2010
Xerostomia
CUI: C0043352
Disease: Xerostomia
1 0.742 0.320 18 12337505 missense variant C/T snv 0.700 1.000 1 2010 2010