Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10741688
rs10741688
SOX6
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
SOX6
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: rs60718933
rs60718933
SOX6
11 16017007 intron variant T/A;C snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2018 2018
dbSNP: rs60718933
rs60718933
SOX6
11 16017007 intron variant T/A;C snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2018 2018
dbSNP: rs1455115
rs1455115
SOX6
11 16193995 intron variant G/A snv 0.54
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1455114
rs1455114
SOX6
0.882 0.200 11 16194000 intron variant C/A snv 0.48
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs1455114
rs1455114
SOX6
0.882 0.200 11 16194000 intron variant C/A snv 0.48
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1837095
rs1837095
SOX6
11 16224146 intron variant T/A snv 0.43
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs12800049
rs12800049
SOX6
11 16227348 intron variant C/T snv 0.20
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs1401454
rs1401454
SOX6
11 16228637 intron variant C/A;G;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2013 2013
dbSNP: rs1401454
rs1401454
SOX6
11 16228637 intron variant C/A;G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2013 2013
dbSNP: rs16932777
rs16932777
SOX6
11 16230637 intron variant C/G snv 0.20
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs10766309
rs10766309
SOX6
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: rs10766309
rs10766309
SOX6
11 16235171 intron variant A/G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs10832571
rs10832571
SOX6
11 16239678 intron variant C/T snv 0.16
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs7118275
rs7118275
SOX6
11 16250132 intron variant C/T snv 0.78
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs7118275
rs7118275
SOX6
11 16250132 intron variant C/T snv 0.78
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs9971406
rs9971406
SOX6
11 16256743 intron variant G/T snv 0.78
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs11023895
rs11023895
SOX6
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: rs11023895
rs11023895
SOX6
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: rs146669915
rs146669915
SOX6
11 16269264 intron variant -/CTGT delins
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2019 2019
dbSNP: rs4757391
rs4757391
SOX6
11 16281393 intron variant C/T snv 0.78
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2015 2017
dbSNP: rs4757391
rs4757391
SOX6
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: rs10832586
rs10832586
SOX6
11 16282543 intron variant A/C;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs1156725
rs1156725
SOX6
11 16286154 intron variant C/T snv 0.78
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016