RXRG, retinoid X receptor gamma, 6258

N. diseases: 40; 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: rs17429130
rs17429130
1 165401015 3 prime UTR variant G/C snv 4.2E-02
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 2016 2016
dbSNP: rs2134095
rs2134095
1.000 0.160 1 165408315 synonymous variant G/A;C snv 0.61; 4.0E-06
CUI: C1708272
Disease: HIV lipodystrophy
HIV lipodystrophy
Nutritional and Metabolic Diseases; Infections; Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10489744
rs10489744
0.925 0.040 1 165411386 intron variant G/A snv 0.55
Attention deficit hyperactivity disorder
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs10489744
rs10489744
0.925 0.040 1 165411386 intron variant G/A snv 0.55
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs3818569
rs3818569
0.925 0.160 1 165419892 synonymous variant G/A snv
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3818569
rs3818569
0.925 0.160 1 165419892 synonymous variant G/A snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs466639
rs466639
1 165425645 intron variant T/A;C snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.800 1.000 2 2010 2014
dbSNP: rs113471
rs113471
1.000 0.160 1 165428878 synonymous variant T/C snv 0.17 0.22
CUI: C1708272
Disease: HIV lipodystrophy
HIV lipodystrophy
Nutritional and Metabolic Diseases; Infections; Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs285480
rs285480
1 165434666 intron variant G/A snv 0.72
CUI: C0233849
Disease: Personality Traits
Personality Traits
Behavior and Behavior Mechanisms 0.800 1.000 1 2011 2011
dbSNP: rs2194899
rs2194899
1.000 0.160 1 165441548 intron variant A/G snv 0.51
CUI: C1708272
Disease: HIV lipodystrophy
HIV lipodystrophy
Nutritional and Metabolic Diseases; Infections; Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2194899
rs2194899
1.000 0.160 1 165441548 intron variant A/G snv 0.51
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs100537
rs100537
1 165444407 intron variant A/G snv 0.60
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2016 2016