CELF2, CUGBP Elav-like family member 2, 10659

N. diseases: 58; N. variants: 22
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: rs62209
rs62209 		1.000 0.080 10 10958376 intron variant G/T snv 0.33
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.800 1.000 1 2011 2011
dbSNP: rs10752212
rs10752212 		1.000 0.040 10 10875158 intron variant G/A snv 0.64
CUI: C0026603
Disease: Motion Sickness
Motion Sickness 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2015 2015
dbSNP: rs11256837
rs11256837 		10 10798572 5 prime UTR variant G/A snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs11257029
rs11257029 		0.925 0.040 10 11241862 intron variant A/G;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11257029
rs11257029 		0.925 0.040 10 11241862 intron variant A/G;T snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1291817
rs1291817 		10 11090087 intron variant A/T snv 0.46
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1291823
rs1291823 		10 11099301 intron variant A/C;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs192238733
rs192238733 		1.000 10 11109944 intron variant G/A snv 4.1E-03
CUI: C0869220
Disease: Adverse effects, not elsewhere classified
Adverse effects, not elsewhere classified 		0.700 1.000 1 2019 2019
dbSNP: rs201099
rs201099 		1.000 0.080 10 10982596 intron variant A/G snv 0.30
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs201109
rs201109 		1.000 0.080 10 11000004 intron variant C/T snv 0.31
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs201119
rs201119 		1.000 0.080 10 11008014 intron variant T/C snv 0.27
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs2765974
rs2765974 		1.000 0.120 10 11246455 intron variant C/A;G snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs596406
rs596406 		10 11182702 intron variant T/C snv 0.15
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2013 2013
dbSNP: rs6602476
rs6602476 		10 11080672 intron variant C/A snv 0.27
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs7083575
rs7083575 		10 11080044 intron variant T/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs769354275
rs769354275 		1.000 0.080 10 10650339 intergenic variant T/G snv 5.0E-04
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2019 2019
dbSNP: rs7904832
rs7904832 		10 10870226 intron variant C/A;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs10905928
rs10905928 		1.000 0.040 10 11300924 intron variant C/A snv 0.21
CUI: C0035222
Disease: Respiratory Distress Syndrome, Adult
Respiratory Distress Syndrome, Adult 		Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2242451
rs2242451 		1.000 0.080 10 11260708 intron variant G/A;C;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs2277212
rs2277212 		1.000 0.040 10 11257772 synonymous variant A/T snv 0.75 0.74
CUI: C0035222
Disease: Respiratory Distress Syndrome, Adult
Respiratory Distress Syndrome, Adult 		Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3740194
rs3740194 		1.000 0.120 10 11255346 intron variant T/C snv 0.47
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3814634
rs3814634 		1.000 0.040 10 11099442 splice region variant G/T snv 0.37
CUI: C0035222
Disease: Respiratory Distress Syndrome, Adult
Respiratory Distress Syndrome, Adult 		Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs7068124
rs7068124 		1.000 0.040 10 11023453 intron variant T/C;G snv
CUI: C0035222
Disease: Respiratory Distress Syndrome, Adult
Respiratory Distress Syndrome, Adult 		Respiratory Tract Diseases 0.010 1.000 1 2016 2016