CELF1, CUGBP Elav-like family member 1, 10658

N. diseases: 63; N. variants: 11
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: rs10838725
rs10838725 		0.925 0.160 11 47536319 intron variant T/C snv 0.22
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.820 1.000 3 2013 2018
dbSNP: rs7124681
rs7124681 		11 47508395 intron variant C/A snv 0.36
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 6 2015 2019
dbSNP: rs11039266
rs11039266 		11 47510843 intron variant T/G snv 0.20
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs11039297
rs11039297 		11 47559891 intron variant G/A snv 0.22
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2018 2018
dbSNP: rs11537751
rs11537751 		11 47565900 missense variant C/T snv 3.7E-02 3.6E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2868996
rs2868996 		11 47553818 intron variant A/T snv 0.31
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs34958982
rs34958982 		11 47525494 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs555328608
rs555328608 		11 47466563 3 prime UTR variant T/-;TT;TTT delins
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs60206633
rs60206633 		11 47552529 intron variant C/A;G snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs61895110
rs61895110 		11 47535608 intron variant G/A snv 4.6E-02
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs7124681
rs7124681 		11 47508395 intron variant C/A snv 0.36
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs77977823
rs77977823 		11 47543586 intron variant T/C snv 2.0E-02
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs10838725
rs10838725 		0.925 0.160 11 47536319 intron variant T/C snv 0.22
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014