LRRC4C, leucine rich repeat containing 4C, 57689

N. diseases: 18; N. variants: 9
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: rs10444280
rs10444280 		11 41134347 intron variant T/C snv 0.20
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs11604865
rs11604865 		1.000 0.080 11 40636452 intron variant T/C snv 0.15
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs11606250
rs11606250 		1.000 0.040 11 40127750 intron variant G/A snv 0.17
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs184852128
rs184852128 		11 40624331 intron variant G/T snv 6.3E-05
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs184852128
rs184852128 		11 40624331 intron variant G/T snv 6.3E-05
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2015 2015
dbSNP: rs2939756
rs2939756 		11 41414747 intron variant G/A snv 0.42
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4611189
rs4611189 		11 40816163 intron variant G/A snv 3.5E-02
CUI: C0684328
Disease: Reasoning
Reasoning 		0.700 1.000 1 2011 2011
dbSNP: rs4612793
rs4612793 		0.925 0.040 11 40890032 intron variant C/T snv 0.95
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs4612793
rs4612793 		0.925 0.040 11 40890032 intron variant C/T snv 0.95
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs729210
rs729210 		11 41237630 intron variant C/T snv 0.19
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs998447
rs998447 		11 40289239 intron variant A/C snv 0.46
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018