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: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.810 1.000 2 2012 2016
dbSNP: rs1847472
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 4 2010 2017
dbSNP: rs11755527
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.800 1.000 3 2008 2011
dbSNP: rs1847472
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 3 2012 2017
dbSNP: rs10806425
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2010 2010
dbSNP: rs12212193
rs12212193
BACH2
0.925 0.280 6 90287050 intron variant A/G snv 0.38
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs2474619
rs2474619
BACH2
0.882 0.360 6 90170316 intron variant C/A snv 0.72
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2014 2014
dbSNP: rs3757247
rs3757247
BACH2
0.827 0.320 6 90247744 intron variant C/T snv 0.38
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.800 1.000 1 2009 2009
dbSNP: rs3757247
rs3757247
BACH2
0.827 0.320 6 90247744 intron variant C/T snv 0.38
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2012 2012
dbSNP: rs7753008
rs7753008
BACH2
1.000 0.080 6 90099920 intron variant T/A;C snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2011 2012
dbSNP: rs58521088
rs58521088
BACH2
0.925 0.080 6 90275479 intron variant A/T snv 0.27
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 2 2016 2019
dbSNP: rs62408225
rs62408225
BACH2
1.000 0.120 6 90246690 intron variant A/G snv 0.26
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs10806425
rs10806425
BACH2
0.851 0.280 6 90216893 intron variant C/A snv 0.33
CUI: C2213246
Disease: Non-Hodgkin's lymphoma of central nervous system
Non-Hodgkin's lymphoma of central nervous system 		0.700 1.000 1 2019 2019
dbSNP: rs11755527
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36
CUI: C1739108
Disease: Latent Autoimmune Diabetes in Adults
Latent Autoimmune Diabetes in Adults 		0.700 1.000 1 2018 2018
dbSNP: rs1504215
rs1504215
BACH2 ; LOC105377891
1.000 0.120 6 90296508 5 prime UTR variant G/A;C snv
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.700 1.000 1 2018 2018
dbSNP: rs17585295
rs17585295
BACH2
6 90235112 intron variant C/T snv 0.27
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs17585295
rs17585295
BACH2
6 90235112 intron variant C/T snv 0.27
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs17765610
rs17765610
BACH2
1.000 0.040 6 89956054 intron variant A/G snv 9.0E-02
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2013 2013
dbSNP: rs182491379
rs182491379
BACH2
6 90129545 intron variant C/T snv 4.3E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1847472
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs1847472
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs1847472
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs1847472
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs206913
rs206913
BACH2
6 90227175 intron variant C/A snv 0.70
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs2134814
rs2134814
BACH2
6 90277793 intron variant C/G snv 0.26
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2017 2017