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: rs78534766
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 2 2017 2017
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 1.000 1 2015 2015
dbSNP: rs78534766
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs78534766
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019
dbSNP: rs78534766
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2017 2017
dbSNP: rs78534766
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs78534766
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs78534766
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019