POU6F2, POU class 6 homeobox 2, 11281

N. diseases: 29; N. variants: 16
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: rs10268735
rs10268735 		7 39336423 intron variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs112503449
rs112503449 		7 39128681 intron variant G/A snv 4.9E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs12674371
rs12674371 		7 39031710 intron variant G/A snv 0.33
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs1558162
rs1558162 		1.000 0.040 7 39471024 intron variant C/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1558162
rs1558162 		1.000 0.040 7 39471024 intron variant C/G;T snv
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2140910
rs2140910 		7 39039873 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2237403
rs2237403 		7 39409337 intron variant C/T snv 0.33
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs28599716
rs28599716 		7 39230866 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs3778934
rs3778934 		7 39405786 intron variant A/C snv 0.34
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs3937443
rs3937443 		1.000 0.040 7 39474399 intron variant T/C snv 0.77
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs3937443
rs3937443 		1.000 0.040 7 39474399 intron variant T/C snv 0.77
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2019 2019
dbSNP: rs4072719
rs4072719 		7 39293971 intron variant C/A snv 0.45
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs58695218
rs58695218 		7 39392731 intron variant A/G snv 0.27
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs60464047
rs60464047 		1.000 0.040 7 39378939 intron variant T/A snv 0.13
CUI: C0026603
Disease: Motion Sickness
Motion Sickness 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2015 2015
dbSNP: rs62443626
rs62443626 		7 39017049 intron variant G/A snv 0.41
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs6952464
rs6952464 		7 39036727 intron variant C/T snv 0.33
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs952623
rs952623 		7 38998316 intron variant G/C snv 0.26
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs121918261
rs121918261 		1.000 0.160 7 39339703 missense variant G/T snv
CUI: C1832099
Disease: Wilms tumor and radial bilateral aplasia
Wilms tumor and radial bilateral aplasia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 0