RARRES2, retinoic acid receptor responder 2, 5919

N. diseases: 180; 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: rs17173608
rs17173608 		0.807 0.240 7 150339575 intron variant T/G snv 0.11
CUI: C0038663
Disease: Suicide attempt
Suicide attempt 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs17173608
rs17173608 		0.807 0.240 7 150339575 intron variant T/G snv 0.11
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs17173608
rs17173608 		0.807 0.240 7 150339575 intron variant T/G snv 0.11
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs3735167
rs3735167 		1.000 0.040 7 150342466 non coding transcript exon variant C/A;G;T snv 0.22
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17173608
rs17173608 		0.807 0.240 7 150339575 intron variant T/G snv 0.11
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.020 1.000 2 2012 2016
dbSNP: rs10278590
rs10278590 		7 150338437 missense variant T/A;C;G snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs17173608
rs17173608 		0.807 0.240 7 150339575 intron variant T/G snv 0.11
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs17173608
rs17173608 		0.807 0.240 7 150339575 intron variant T/G snv 0.11
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs17173608
rs17173608 		0.807 0.240 7 150339575 intron variant T/G snv 0.11
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2018 2018
dbSNP: rs17173608
rs17173608 		0.807 0.240 7 150339575 intron variant T/G snv 0.11
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3735167
rs3735167 		1.000 0.040 7 150342466 non coding transcript exon variant C/A;G;T snv 0.22
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs4721
rs4721 		1.000 0.040 7 150338437 missense variant T/A;C;G snv 0.42 0.47
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		Musculoskeletal Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4721
rs4721 		1.000 0.040 7 150338437 missense variant T/A;C;G snv 0.42 0.47
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2018 2018