Source: ALL

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: rs2024714
rs2024714
CDH4
20 61637438 intron variant C/T snv 0.60
CUI: C0023980
Disease: Longevity
Longevity 		0.800 1.000 1 2010 2010
dbSNP: rs4468878
rs4468878
CDH4
20 61353181 intron variant T/C snv 0.51
CUI: C0023980
Disease: Longevity
Longevity 		0.800 1.000 1 2010 2010
dbSNP: rs143502921
rs143502921
CDH4
1.000 0.040 20 61252175 upstream gene variant G/A;C;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs150734585
rs150734585
CDH4
1.000 0.040 20 61333207 intron variant G/A;C snv
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.700 1.000 1 2015 2015
dbSNP: rs2427216
rs2427216
CDH4
1.000 0.040 20 61639158 intron variant C/A;T snv
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		0.700 1.000 1 2008 2008
dbSNP: rs6028083
rs6028083
CDH4
20 61263043 intron variant T/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs6061910
rs6061910
CDH4
20 61933124 splice region variant G/A snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs78897171
rs78897171
CDH4
1.000 0.080 20 61868195 intron variant G/A snv 4.8E-02
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		0.700 1.000 1 2016 2016
dbSNP: rs765815715
rs765815715
CDH4
20 61928394 missense variant G/A;C snv 2.0E-05
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		0.700 0