ERG, ETS transcription factor ERG, 2078

N. diseases: 298; N. variants: 31
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: rs2836411
rs2836411 		1.000 0.040 21 38447907 intron variant C/A;T snv
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
Aortic Aneurysm, Abdominal 		Cardiovascular Diseases 0.720 1.000 3 2017 2020
dbSNP: rs2836425
rs2836425 		1.000 0.080 21 38466902 intron variant C/T snv 0.11
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.710 1.000 2 2016 2019
dbSNP: rs117870289
rs117870289 		21 38611524 intron variant C/T snv 7.7E-03
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2017 2019
dbSNP: rs2836422
rs2836422 		21 38466112 intron variant T/A snv 0.46
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs1015022
rs1015022 		21 38507058 intron variant G/C snv 0.26
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs117870289
rs117870289 		21 38611524 intron variant C/T snv 7.7E-03
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs117910189
rs117910189 		21 38606304 intron variant T/C snv 1.6E-02
CUI: C1318312
Disease: Serum iron measurement
Serum iron measurement 		0.700 1.000 1 2017 2017
dbSNP: rs2836389
rs2836389 		1.000 0.080 21 38431740 intron variant T/C snv 0.27
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.700 1.000 1 2011 2011
dbSNP: rs2836422
rs2836422 		21 38466112 intron variant T/A snv 0.46
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs2836439
rs2836439 		1.000 0.040 21 38493226 intron variant C/T snv 0.16
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs2836441
rs2836441 		21 38498386 5 prime UTR variant G/A snv 0.87 0.89
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs35042034
rs35042034 		21 38465700 intron variant G/A snv 0.18
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs56180262
rs56180262 		21 38433581 intron variant G/A snv 0.19
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs58030288
rs58030288 		21 38482555 intron variant C/A;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs58030288
rs58030288 		21 38482555 intron variant C/A;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7275212
rs7275212 		21 38480628 intron variant A/T snv 2.9E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2011 2011
dbSNP: rs7275212
rs7275212 		21 38480628 intron variant A/T snv 2.9E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs78762153
rs78762153 		21 38473352 intron variant T/C snv 1.5E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2018 2018
dbSNP: rs80109907
rs80109907 		21 38479032 intron variant C/A snv 2.0E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9977881
rs9977881 		0.925 0.040 21 38635298 intron variant T/C;G snv
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9977881
rs9977881 		0.925 0.040 21 38635298 intron variant T/C;G snv
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9982370
rs9982370 		21 38493931 intron variant C/T snv 0.22
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs1004072779
rs1004072779 		0.925 0.080 21 38403547 missense variant T/C snv 2.1E-05
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1004072779
rs1004072779 		0.925 0.080 21 38403547 missense variant T/C snv 2.1E-05
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1168030806
rs1168030806 		1.000 0.040 21 38392384 missense variant T/C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.010 1.000 1 2010 2010