CDH15, cadherin 15, 1013

N. diseases: 38; N. variants: 5
Source: ALL
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: rs121434539
rs121434539
1.000 0.160 16 89179551 missense variant C/T snv 1.2E-04 7.7E-05
Mental Retardation, Autosomal Dominant 3
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 1.000 1 2008 2008
dbSNP: rs66682219
rs66682219
16 89187202 intron variant A/G snv 0.16
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs121434540
rs121434540
1.000 0.160 16 89180272 missense variant C/T snv 5.4E-05 1.1E-04
Mental Retardation, Autosomal Dominant 3
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs121434541
rs121434541
1.000 0.160 16 89183555 missense variant C/T snv 2.0E-04 6.6E-04
Mental Retardation, Autosomal Dominant 3
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0
dbSNP: rs567903921
rs567903921
1.000 0.160 16 89171853 missense variant G/C snv 1.3E-04 1.6E-04
Mental Retardation, Autosomal Dominant 3
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms 0.700 0