RORA, RAR related orphan receptor A, 6095

N. diseases: 158; N. variants: 54
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: rs11071559
rs11071559 		0.925 0.080 15 60777789 intron variant C/T snv 0.23
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.820 1.000 7 2010 2019
dbSNP: rs3743266
rs3743266 		15 60489314 3 prime UTR variant T/C snv 0.31
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.800 1.000 3 2010 2019
dbSNP: rs339969
rs339969 		15 60591082 intron variant C/A snv 0.68
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.800 1.000 2 2011 2018
dbSNP: rs340005
rs340005 		15 60585831 intron variant G/A snv 0.67
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.800 1.000 2 2012 2019
dbSNP: rs340029
rs340029 		15 60602766 intron variant C/T snv 0.70
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.800 1.000 1 2011 2011
dbSNP: rs8042149
rs8042149 		0.882 0.160 15 60832754 intron variant T/G snv 0.44
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		Mental Disorders 0.720 1.000 3 2013 2019
dbSNP: rs4775319
rs4775319 		0.925 0.040 15 60921365 intron variant G/A snv 0.62
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm 		Neoplasms 0.710 1.000 1 2018 2018
dbSNP: rs10519068
rs10519068 		0.925 0.120 15 60776505 intron variant G/A snv 0.22
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 2 2016 2019
dbSNP: rs11071559
rs11071559 		0.925 0.080 15 60777789 intron variant C/T snv 0.23
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 2 2019 2019
dbSNP: rs17237465
rs17237465 		15 60897812 intron variant T/C snv 0.31
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 2 2018 2019
dbSNP: rs340005
rs340005 		15 60585831 intron variant G/A snv 0.67
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 2 2016 2018
dbSNP: rs8033510
rs8033510 		15 61153315 intron variant T/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs10519067
rs10519067 		0.925 0.120 15 60776148 intron variant G/A snv 0.20
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs10519067
rs10519067 		0.925 0.120 15 60776148 intron variant G/A snv 0.20
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs10519067
rs10519067 		0.925 0.120 15 60776148 intron variant G/A snv 0.20
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2018 2018
dbSNP: rs10519068
rs10519068 		0.925 0.120 15 60776505 intron variant G/A snv 0.22
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs11071558
rs11071558 		1.000 0.080 15 60777222 intron variant A/C;G snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11071559
rs11071559 		0.925 0.080 15 60777789 intron variant C/T snv 0.23
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs11071559
rs11071559 		0.925 0.080 15 60777789 intron variant C/T snv 0.23
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs12594733
rs12594733 		15 60952685 intron variant T/C snv 0.25
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2014 2014
dbSNP: rs12594733
rs12594733 		15 60952685 intron variant T/C snv 0.25
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2014 2014
dbSNP: rs12912233
rs12912233 		0.851 0.120 15 60974897 intron variant C/T snv 0.38
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2010 2010
dbSNP: rs12916023
rs12916023 		15 61163854 intron variant A/G snv 0.47
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1433850094
rs1433850094 		1.000 15 60499914 missense variant C/T snv 4.0E-06
CUI: C4748041
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA
INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA 		0.700 1.000 1 2018 2018
dbSNP: rs1555427497
rs1555427497 		1.000 15 60531767 missense variant T/C snv
CUI: C4748041
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA
INTELLECTUAL DEVELOPMENTAL DISORDER WITH OR WITHOUT EPILEPSY OR CEREBELLAR ATAXIA 		0.700 1.000 1 2018 2018