Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16942585
rs16942585
CDH8
0.925 0.040 16 61989866 intron variant C/T snv 0.16
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs16942585
rs16942585
CDH8
0.925 0.040 16 61989866 intron variant C/T snv 0.16
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs200312707
rs200312707
CDH8
1.000 0.040 16 62031776 intron variant TA/- del
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2016 2016
dbSNP: rs200312707
rs200312707
CDH8
1.000 0.040 16 62031776 intron variant TA/- del
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2016 2016
dbSNP: rs3784847
rs3784847
CDH8
1.000 0.040 16 61943545 intron variant A/G snv 9.5E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2011 2011
dbSNP: rs78513878
rs78513878
CDH8
16 61755851 intron variant C/T snv 0.16
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs968627
rs968627
CDH8
16 62019156 intron variant A/G snv 0.57
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018