Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs587777161
rs587777161
1.000 X 10213734 missense variant G/A;C snv
CUI: C1843367
Disease: Poor school performance
Poor school performance
0.700 1.000 1 2018 2018
dbSNP: rs879255580
rs879255580
X 10206437 missense variant T/G snv
CUI: C1843367
Disease: Poor school performance
Poor school performance
0.700 1.000 1 2018 2018
dbSNP: rs879255581
rs879255581
X 10206464 missense variant T/C snv
CUI: C1843367
Disease: Poor school performance
Poor school performance
0.700 1.000 1 2018 2018
dbSNP: rs879255582
rs879255582
X 10213705 missense variant C/T snv
CUI: C1843367
Disease: Poor school performance
Poor school performance
0.700 1.000 1 2018 2018
dbSNP: rs879255583
rs879255583
X 10213768 missense variant C/T snv
CUI: C1843367
Disease: Poor school performance
Poor school performance
0.700 1.000 1 2018 2018
dbSNP: rs879255584
rs879255584
X 10220837 missense variant C/T snv
CUI: C1843367
Disease: Poor school performance
Poor school performance
0.700 1.000 1 2018 2018
dbSNP: rs879255585
rs879255585
X 10206756 missense variant G/A snv
CUI: C1843367
Disease: Poor school performance
Poor school performance
0.700 1.000 1 2018 2018
dbSNP: rs879255586
rs879255586
X 10213979 frameshift variant -/A delins
CUI: C1843367
Disease: Poor school performance
Poor school performance
0.700 1.000 1 2018 2018
dbSNP: rs879255590
rs879255590
X 10208595 splice region variant G/A snv
CUI: C1843367
Disease: Poor school performance
Poor school performance
0.700 1.000 1 2018 2018