MYO9B, myosin IXB, 4650

N. diseases: 65; N. variants: 29
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: rs11086054
rs11086054 		19 17135927 intron variant A/C;T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2018 2018
dbSNP: rs11666569
rs11666569 		1.000 0.080 19 17103263 non coding transcript exon variant C/T snv 0.33
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11881955
rs11881955 		19 17143698 intron variant A/G snv 0.49
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs11881955
rs11881955 		19 17143698 intron variant A/G snv 0.49
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2017 2017
dbSNP: rs12982956
rs12982956 		19 17127603 intron variant A/G snv 0.25
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1379281
rs1379281 		19 17078976 intron variant G/A snv 0.36
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs144744357
rs144744357 		19 17084024 intron variant TTAATAACCCTTTGGG/-;TTAATAACCCTTTGGGTTAATAACCCTTTGGG delins
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs188493101
rs188493101 		19 17184193 intron variant G/T snv 1.4E-05
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs188493101
rs188493101 		19 17184193 intron variant G/T snv 1.4E-05
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs2279008
rs2279008 		19 17172493 intron variant T/C snv 0.25 0.23
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs2279008
rs2279008 		19 17172493 intron variant T/C snv 0.25 0.23
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2010 2010
dbSNP: rs2305769
rs2305769 		19 17154151 intron variant G/C snv 0.21
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs34831515
rs34831515 		19 17164967 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs35365035
rs35365035 		19 17141341 intron variant T/C snv 0.49
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs35365035
rs35365035 		19 17141341 intron variant T/C snv 0.49
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs3745348
rs3745348 		1.000 0.040 19 17101600 intron variant C/T snv 0.38
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs3745348
rs3745348 		1.000 0.040 19 17101600 intron variant C/T snv 0.38
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs4808569
rs4808569 		19 17108160 intron variant C/A snv 0.15
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs4808569
rs4808569 		19 17108160 intron variant C/A snv 0.15
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs4808579
rs4808579 		19 17144924 intron variant T/A;C snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs4808579
rs4808579 		19 17144924 intron variant T/A;C snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs59616136
rs59616136 		19 17141231 intron variant G/A snv 8.1E-02
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs59616136
rs59616136 		19 17141231 intron variant G/A snv 8.1E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs59616136
rs59616136 		19 17141231 intron variant G/A snv 8.1E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs59616136
rs59616136 		19 17141231 intron variant G/A snv 8.1E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016