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: rs1156725
rs1156725
SOX6
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: rs12799126
rs12799126
SOX6
11 16286917 intron variant G/T snv 0.17
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs12799126
rs12799126
SOX6
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
SOX6
11 16286917 intron variant G/T snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs893311
rs893311
SOX6
11 16296972 intron variant G/T snv 0.16
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs893311
rs893311
SOX6
11 16296972 intron variant G/T snv 0.16
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs11023906
rs11023906
SOX6
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
SOX6
11 16302860 intron variant G/A snv 0.17
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs11023906
rs11023906
SOX6
11 16302860 intron variant G/A snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2218001
rs2218001
SOX6
11 16320669 intron variant A/C;G;T snv
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2218001
rs2218001
SOX6
11 16320669 intron variant A/C;G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2018 2018
dbSNP: rs7131442
rs7131442
SOX6
11 16326515 intron variant A/T snv 0.17
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs7131442
rs7131442
SOX6
11 16326515 intron variant A/T snv 0.17
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs12801635
rs12801635
SOX6
11 16330999 intron variant T/C snv 0.17
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs297346
rs297346
SOX6
1.000 0.040 11 16334225 intron variant A/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs297346
rs297346
SOX6
1.000 0.040 11 16334225 intron variant A/G;T snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs17462448
rs17462448
SOX6
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: rs17462448
rs17462448
SOX6
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
SOX6
11 16338021 intron variant G/A snv 5.6E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs2014408
rs2014408
SOX6
11 16343736 intron variant C/T snv 0.17
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2014408
rs2014408
SOX6
11 16343736 intron variant C/T snv 0.17
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs75491173
rs75491173
SOX6
11 16346948 intron variant G/A snv 3.1E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs7109376
rs7109376
SOX6
11 16350885 intron variant T/A snv 0.29
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs297325
rs297325
SOX6
0.925 0.120 11 16368048 intron variant T/C;G snv
CUI: C0028754
Disease: Obesity
Obesity 		0.700 1.000 1 2009 2009
dbSNP: rs297325
rs297325
SOX6
0.925 0.120 11 16368048 intron variant T/C;G snv
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.700 1.000 1 2009 2009