SDK1, sidekick cell adhesion molecule 1, 221935

N. diseases: 18; N. variants: 41
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: rs10085617
rs10085617 		1.000 7 3595079 intron variant A/T snv 0.66
CUI: C3160814
Disease: Cannabis use
Cannabis use 		0.700 1.000 1 2018 2018
dbSNP: rs1019914
rs1019914 		7 3672560 intron variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs10951155
rs10951155 		7 3320052 intron variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1108879
rs1108879 		7 3516500 intron variant G/A snv 0.61
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs117749317
rs117749317 		7 4234812 intron variant G/A snv 1.6E-02
CUI: C0523953
Disease: Cardiac troponin T measurement
Cardiac troponin T measurement 		0.700 1.000 1 2019 2019
dbSNP: rs13237637
rs13237637 		7 3463575 intron variant G/C snv 0.40
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs17133347
rs17133347 		7 3433089 intron variant C/A;G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4257931
rs4257931 		7 3603698 intron variant G/A snv 0.52
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4336505
rs4336505 		7 3334108 intron variant A/C;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4719944
rs4719944 		7 3456400 intron variant T/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs645106
rs645106 		7 4150281 intron variant T/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs6462203
rs6462203 		7 3636370 intron variant C/A;T snv
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs6462411
rs6462411 		7 3875932 intron variant T/C snv 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2009 2009
dbSNP: rs6462411
rs6462411 		7 3875932 intron variant T/C snv 0.34
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		0.700 1.000 1 2009 2009
dbSNP: rs959894
rs959894 		7 3621401 intron variant T/A;G snv 0.66
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs10242223
rs10242223 		1.000 0.040 7 3481941 intron variant A/G;T snv
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		Digestive System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs17134117
rs17134117 		1.000 0.040 7 3991432 intron variant C/T snv 9.1E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.700 1.000 1 2013 2013
dbSNP: rs34912216
rs34912216 		1.000 0.040 7 4078745 intron variant G/A snv 0.37
CUI: C0026603
Disease: Motion Sickness
Motion Sickness 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2015 2015
dbSNP: rs4343996
rs4343996 		1.000 0.040 7 3323010 intron variant G/A;C;T snv
CUI: C0026603
Disease: Motion Sickness
Motion Sickness 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2015 2015
dbSNP: rs10226621
rs10226621 		1.000 0.080 7 4068008 intron variant A/C;G snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs10234405
rs10234405 		1.000 0.080 7 4034827 intron variant A/G snv 0.33
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs10237319
rs10237319 		1.000 0.080 7 4033969 intron variant C/T snv 0.25
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs10237488
rs10237488 		1.000 0.080 7 4034710 intron variant T/G snv 0.33
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs10237838
rs10237838 		1.000 0.080 7 4034366 intron variant C/T snv 0.34
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs10265937
rs10265937 		1.000 0.080 7 4034017 intron variant G/A snv 0.32
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012