RBFOX1, RNA binding fox-1 homolog 1, 54715

N. diseases: 103; N. variants: 76
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: rs11645781
rs11645781 		16 6846127 intron variant A/C;G;T snv
CUI: C0018810
Disease: heart rate
heart rate 		0.800 1.000 1 2013 2013
dbSNP: rs4787008
rs4787008 		1.000 0.120 16 7365551 intron variant A/G snv 0.87
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.800 1.000 1 2011 2011
dbSNP: rs870288
rs870288 		16 5535851 intron variant A/G snv 0.30
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.800 1.000 1 2012 2012
dbSNP: rs7193263
rs7193263 		1.000 0.040 16 6265879 intron variant G/A snv 0.52
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 2 2018 2019
dbSNP: rs7198928
rs7198928 		1.000 0.040 16 7616400 intron variant T/A;C snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 2 2018 2019
dbSNP: rs10500355
rs10500355 		0.925 0.040 16 7409346 intron variant T/A snv 0.29
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs10500355
rs10500355 		0.925 0.040 16 7409346 intron variant T/A snv 0.29
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction 		0.700 1.000 1 2013 2013
dbSNP: rs10500355
rs10500355 		0.925 0.040 16 7409346 intron variant T/A snv 0.29
CUI: C0034951
Disease: Refractive Errors
Refractive Errors 		Eye Diseases 0.700 1.000 1 2013 2013
dbSNP: rs10775354
rs10775354 		1.000 0.080 16 6757689 intron variant A/C;T snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs11076962
rs11076962 		16 5761366 intron variant T/C snv 0.25
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs11076962
rs11076962 		16 5761366 intron variant T/C snv 0.25
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs11077204
rs11077204 		16 7617185 intron variant C/A;G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs11077207
rs11077207 		16 7618478 intron variant C/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs11642387
rs11642387 		16 6703238 intron variant A/G snv 6.7E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11643447
rs11643447 		16 6649260 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2012 2012
dbSNP: rs11646221
rs11646221 		16 7616086 intron variant G/T snv 0.47
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs11865256
rs11865256 		16 7215069 intron variant C/T snv 0.38
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs12446308
rs12446308 		1.000 0.080 16 6367932 intron variant A/G snv 8.8E-02
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2009 2009
dbSNP: rs12447542
rs12447542 		1.000 0.040 16 7694178 intron variant G/A snv 9.2E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs12597084
rs12597084 		1.000 0.120 16 5769619 intron variant A/C snv 0.67
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs12709186
rs12709186 		16 7199471 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs12923795
rs12923795 		1.000 0.040 16 7612705 intron variant A/C;G snv
CUI: C0003467
Disease: Anxiety
Anxiety 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs12933772
rs12933772 		16 6510429 intron variant C/G snv 0.23
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs13332522
rs13332522 		1.000 0.040 16 5779203 intron variant G/A;C snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs13337052
rs13337052 		0.925 0.040 16 7323469 intron variant T/C snv 0.23
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018