SOX6, SRY-box transcription factor 6, 55553

N. diseases: 105; N. variants: 46
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: rs17462448
rs17462448 		11 16338021 intron variant G/A snv 5.6E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 2 2016 2017
dbSNP: rs17462448
rs17462448 		11 16338021 intron variant G/A snv 5.6E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 2 2016 2017
dbSNP: rs4757391
rs4757391 		11 16281393 intron variant C/T snv 0.78
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 2 2015 2017
dbSNP: rs4757391
rs4757391 		11 16281393 intron variant C/T snv 0.78
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2015 2017
dbSNP: rs10741688
rs10741688 		11 15990568 intron variant A/C;T snv 0.51
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: rs10741688
rs10741688 		11 15990568 intron variant A/C;T snv 0.51
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs10766309
rs10766309 		11 16235171 intron variant A/G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs10766309
rs10766309 		11 16235171 intron variant A/G;T snv
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs10832571
rs10832571 		11 16239678 intron variant C/T snv 0.16
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs10832586
rs10832586 		11 16282543 intron variant A/C;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs10832648
rs10832648 		11 16596760 intron variant C/A snv 0.26
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs11023895
rs11023895 		11 16264638 3 prime UTR variant G/A;C snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs11023895
rs11023895 		11 16264638 3 prime UTR variant G/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: rs11023906
rs11023906 		11 16302860 intron variant G/A snv 0.17
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11023906
rs11023906 		11 16302860 intron variant G/A snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs11023906
rs11023906 		11 16302860 intron variant G/A snv 0.17
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs1156725
rs1156725 		11 16286154 intron variant C/T snv 0.78
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs1156725
rs1156725 		11 16286154 intron variant C/T snv 0.78
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		0.700 1.000 1 2011 2011
dbSNP: rs1156725
rs1156725 		11 16286154 intron variant C/T snv 0.78
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs12365482
rs12365482 		11 16591389 intron variant A/T snv 0.25
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs12799126
rs12799126 		11 16286917 intron variant G/T snv 0.17
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs12799126
rs12799126 		11 16286917 intron variant G/T snv 0.17
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs12799126
rs12799126 		11 16286917 intron variant G/T snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs12800049
rs12800049 		11 16227348 intron variant C/T snv 0.20
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs12801635
rs12801635 		11 16330999 intron variant T/C snv 0.17
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018