DCC, DCC netrin 1 receptor, 1630

N. diseases: 279; N. variants: 101
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: rs12968428
rs12968428 		1.000 0.040 18 53223855 intron variant A/G snv 0.33
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs13381096
rs13381096 		18 53423032 intron variant C/A snv 0.31
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs1346972
rs1346972 		0.925 0.040 18 52768791 intron variant G/A snv 2.0E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1346972
rs1346972 		0.925 0.040 18 52768791 intron variant G/A snv 2.0E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1367633
rs1367633 		18 53221586 intron variant G/A snv 0.36
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs1431181
rs1431181 		1.000 0.040 18 53253042 intron variant G/A snv 0.30
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs1431196
rs1431196 		1.000 0.040 18 53305732 intron variant A/G snv 0.31 0.30
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs149735550
rs149735550 		1.000 0.040 18 52866733 intron variant G/T snv 0.30
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs1502233
rs1502233 		18 53464065 intron variant T/C snv 0.58
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs1555652216
rs1555652216 		1.000 18 53322064 missense variant C/A snv
CUI: C4479640
Disease: GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2
GAZE PALSY, FAMILIAL HORIZONTAL, WITH PROGRESSIVE SCOLIOSIS, 2 		0.700 1.000 1 2017 2017
dbSNP: rs16955886
rs16955886 		0.925 0.040 18 52943172 intron variant A/G snv 6.0E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs16955886
rs16955886 		0.925 0.040 18 52943172 intron variant A/G snv 6.0E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs17410557
rs17410557 		1.000 0.040 18 53250021 intron variant T/C snv 0.28
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs17411061
rs17411061 		18 53268743 intron variant C/T snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs17417046
rs17417046 		18 53458627 intron variant C/T snv 0.33
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs17468382
rs17468382 		1.000 0.040 18 52734641 intron variant T/C snv 3.7E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs17487484
rs17487484 		1.000 0.040 18 53196913 intron variant T/A;G snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs17487484
rs17487484 		1.000 0.040 18 53196913 intron variant T/A;G snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs17669415
rs17669415 		18 52358627 intron variant C/G;T snv
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs17748074
rs17748074 		18 52420925 intron variant A/G;T snv
CUI: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy 		Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs17748074
rs17748074 		18 52420925 intron variant A/G;T snv
CUI: C4721453
Disease: Peripheral Nervous System Diseases
Peripheral Nervous System Diseases 		Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1875560
rs1875560 		1.000 0.040 18 53434318 intron variant A/C;G snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs1875560
rs1875560 		1.000 0.040 18 53434318 intron variant A/C;G snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs1972044
rs1972044 		18 53404710 intron variant G/A snv 0.32
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2229080
rs2229080 		0.742 0.320 18 52906232 missense variant C/A;G snv 0.45
CUI: C0220611
Disease: Childhood Rhabdomyosarcoma
Childhood Rhabdomyosarcoma 		Neoplasms 0.010 1.000 1 2000 2000