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: rs376898975
rs376898975
C11orf58 ; SOX6
11 16737518 intron variant A/-;AA;AAA;AAAAA delins
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs3809095
rs3809095
C11orf58 ; SOX6
11 16736699 intron variant A/G snv 0.21
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs7482541
rs7482541
C11orf58 ; SOX6 ; LOC105376571
11 16642576 intron variant T/C snv 0.34
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs7482541
rs7482541
C11orf58 ; SOX6 ; LOC105376571
11 16642576 intron variant T/C snv 0.34
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs55941903
rs55941903
C11orf58 ; SOX6 ; LOC105376571
11 16623133 intron variant A/C snv 0.34
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs4756856
rs4756856
C11orf58 ; SOX6 ; LOC105376571
11 16620171 intron variant T/G snv 0.34
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs35199438
rs35199438
SOX6
11 16609232 intron variant G/T snv 0.28
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs10832648
rs10832648
SOX6
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: rs12365482
rs12365482
SOX6
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: rs7943712
rs7943712
SOX6
11 16522316 intron variant G/A snv 0.24
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs34156428
rs34156428
SOX6
1.000 0.040 11 16460403 intron variant A/T snv 0.15
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs72871339
rs72871339
SOX6
11 16388953 intron variant C/T snv 1.8E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs4756846
rs4756846
SOX6
0.925 0.120 11 16381965 intron variant T/C snv 8.8E-02
CUI: C0028754
Disease: Obesity
Obesity 		0.700 1.000 1 2009 2009
dbSNP: rs4756846
rs4756846
SOX6
0.925 0.120 11 16381965 intron variant T/C snv 8.8E-02
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.700 1.000 1 2009 2009
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
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: 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: 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: 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: 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