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: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 2 2016 2019
dbSNP: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs10748781
rs10748781 		0.763 0.160 10 99523573 upstream gene variant C/A;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016