USP3, ubiquitin specific peptidase 3, 9960

N. diseases: 32; N. variants: 10
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: rs2058914
rs2058914 		15 63539785 intron variant G/A snv 0.68
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 2 2018 2019
dbSNP: rs11638671
rs11638671 		15 63503429 upstream gene variant T/C snv 0.25
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12907106
rs12907106 		15 63581459 intron variant C/G snv 0.69
CUI: C0202231
Disease: Thyroxine measurement
Thyroxine measurement 		0.700 1.000 1 2018 2018
dbSNP: rs146311723
rs146311723 		1.000 0.080 15 63512308 intron variant T/C snv 0.14
CUI: C0001925
Disease: Albuminuria
Albuminuria 		Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs146311723
rs146311723 		1.000 0.080 15 63512308 intron variant T/C snv 0.14
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs34262657
rs34262657 		15 63557088 intron variant T/G snv 4.5E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs35639661
rs35639661 		15 63506371 intron variant AAAA/-;AA;AAA;AAAAA delins
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs55848327
rs55848327 		15 63527228 intron variant G/A snv 0.74
CUI: C1629609
Disease: Age at menopause
Age at menopause 		0.700 1.000 1 2019 2019
dbSNP: rs62011291
rs62011291 		1.000 0.080 15 63507814 intron variant A/G snv 0.16
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs6494407
rs6494407 		15 63511630 intron variant A/G snv 0.60
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs982077
rs982077 		1.000 0.080 15 63531102 intron variant A/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2018 2018