rs730882226, INO80

N. diseases: 3
Source: CLINVAR ×
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.
Epilepsy
CUI: C0014544
Disease: Epilepsy
36 0.925 0.120 15 41071953 missense variant A/G snv 1.6E-05 4.2E-05 0.700 0
Poor school performance
CUI: C1843367
Disease: Poor school performance
411 0.925 0.120 15 41071953 missense variant A/G snv 1.6E-05 4.2E-05 0.700 0
Primary microcephaly
CUI: C0431350
Disease: Primary microcephaly
7 0.925 0.120 15 41071953 missense variant A/G snv 1.6E-05 4.2E-05 0.700 0