NCL, nucleolin, 4691

N. diseases: 167; N. variants: 4
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: rs16828074
rs16828074 		1.000 0.040 2 231454043 3 prime UTR variant C/G;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.800 1.000 1 2013 2013
dbSNP: rs10202701
rs10202701 		2 231463970 5 prime UTR variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6737291
rs6737291 		2 231464848 intron variant T/C snv 0.52
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7598759
rs7598759 		1.000 0.120 2 231457245 non coding transcript exon variant C/T snv 0.45 0.46
CUI: C0018781
Disease: Noise-induced hearing loss
Noise-induced hearing loss 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2015 2015