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: rs676556
rs676556
BBX
3 107648872 intron variant A/G snv 0.23
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 2 2018 2019
dbSNP: rs13060816
rs13060816
BBX
1.000 0.040 3 107561639 intron variant T/A;C snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs13060816
rs13060816
BBX
1.000 0.040 3 107561639 intron variant T/A;C snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs28447555
rs28447555
BBX
3 107666821 intron variant C/T snv 0.12
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs600011
rs600011
BBX
1.000 0.040 3 107576545 intron variant A/C snv 0.25
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs600011
rs600011
BBX
1.000 0.040 3 107576545 intron variant A/C snv 0.25
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs6437740
rs6437740
BBX
3 107746970 intron variant T/C snv 0.25
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2009 2009
dbSNP: rs670752
rs670752
BBX
3 107594133 intron variant G/A;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs670752
rs670752
BBX
3 107594133 intron variant G/A;T snv
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2017 2017
dbSNP: rs6782394
rs6782394
BBX
3 107680282 intron variant A/G snv 0.35
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs75774080
rs75774080
BBX
3 107655793 intron variant C/T snv 0.12
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs9839653
rs9839653
BBX
3 107621922 intron variant A/C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs9846246
rs9846246
BBX
1.000 0.080 3 107705243 intron variant G/A;T snv
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs9868075
rs9868075
BBX
1.000 0.040 3 107549762 intron variant C/T snv 0.13
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs9868075
rs9868075
BBX
1.000 0.040 3 107549762 intron variant C/T snv 0.13
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs9869574
rs9869574
BBX
3 107662804 5 prime UTR variant A/C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019