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: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.700 1.000 1 2016 2016
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2016 2016
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		0.700 1.000 1 2012 2012
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2012 2012
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2012 2012
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.700 1.000 1 2013 2013
dbSNP: rs72928038
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019