CTBP2, C-terminal binding protein 2, 1488

N. diseases: 62; N. variants: 13
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: rs4962416
rs4962416 		0.882 0.160 10 125008303 intron variant T/C snv 0.23
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.720 1.000 4 2008 2018
dbSNP: rs4962416
rs4962416 		0.882 0.160 10 125008303 intron variant T/C snv 0.23
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.720 1.000 3 2008 2016
dbSNP: rs1561589
rs1561589 		10 125007104 intron variant G/A snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2018 2019
dbSNP: rs10901868
rs10901868 		10 125135397 intron variant T/C snv 0.45
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1915146
rs1915146 		10 125157645 intron variant A/C;G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs2919290
rs2919290 		10 125049964 intron variant T/A snv 0.57
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2946994
rs2946994 		10 125026145 missense variant G/C;T snv 0.48; 4.1E-06
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs35106605
rs35106605 		10 125154732 intron variant T/G snv 0.15
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs3781411
rs3781411 		10 125026867 missense variant C/T snv 0.15 0.14
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3781426
rs3781426 		10 125014780 intron variant C/T snv 0.27
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2015 2015
dbSNP: rs4021186
rs4021186 		10 125073268 intron variant C/A;T snv 0.61
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs4411245
rs4411245 		10 125024212 intron variant G/A snv 0.27
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs4962416
rs4962416 		0.882 0.160 10 125008303 intron variant T/C snv 0.23
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2010 2010
dbSNP: rs57592469
rs57592469 		10 125161920 upstream gene variant A/G snv 0.47
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs718948
rs718948 		10 125050769 intron variant T/C snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015