RXRA, retinoid X receptor alpha, 6256

N. diseases: 132; N. variants: 23
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: rs34312136
rs34312136 		9 134377610 intron variant T/C snv 0.42
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.800 1.000 1 2012 2012
dbSNP: rs10120653
rs10120653 		9 134415237 intron variant G/T snv 1.2E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10120653
rs10120653 		9 134415237 intron variant G/T snv 1.2E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10120653
rs10120653 		9 134415237 intron variant G/T snv 1.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10125024
rs10125024 		9 134407131 intron variant C/T snv 1.5E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1057519958
rs1057519958 		0.851 0.200 9 134436505 missense variant C/A;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs1057519958
rs1057519958 		0.851 0.200 9 134436505 missense variant C/A;T snv
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
Transitional cell carcinoma of bladder 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1057519958
rs1057519958 		0.851 0.200 9 134436505 missense variant C/A;T snv
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas 		Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11102986
rs11102986 		9 134393657 intron variant A/G snv 0.86
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2012 2012
dbSNP: rs34090729
rs34090729 		9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34090729
rs34090729 		9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34090729
rs34090729 		9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34090729
rs34090729 		9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34090729
rs34090729 		9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34090729
rs34090729 		9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34186206
rs34186206 		9 134410058 intron variant C/T snv 1.8E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34986018
rs34986018 		9 134433616 intron variant G/A snv 1.2E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs34986018
rs34986018 		9 134433616 intron variant G/A snv 1.2E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35079168
rs35079168 		9 134389093 intron variant G/A snv 0.52
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2012 2012
dbSNP: rs35738419
rs35738419 		9 134411944 intron variant C/T snv 7.3E-04
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35738419
rs35738419 		9 134411944 intron variant C/T snv 7.3E-04
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35738419
rs35738419 		9 134411944 intron variant C/T snv 7.3E-04
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35738419
rs35738419 		9 134411944 intron variant C/T snv 7.3E-04
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35738419
rs35738419 		9 134411944 intron variant C/T snv 7.3E-04
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4501664
rs4501664 		9 134393077 intron variant G/A snv 1.6E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2012 2012