ADCY7, adenylate cyclase 7, 113

N. diseases: 38; N. variants: 2
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs78534766
rs78534766
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1.000 2 2017 2017
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0033860
Disease: Psoriasis
Psoriasis
Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
Musculoskeletal Diseases 0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
Digestive System Diseases; Nutritional and Metabolic Diseases 0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency
Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs77150043
rs77150043
0.724 0.240 16 50270338 intron variant C/T snv 0.17
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs78534766
rs78534766
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs78534766
rs78534766
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2019 2019
dbSNP: rs78534766
rs78534766
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2019 2019
dbSNP: rs78534766
rs78534766
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2019 2019
dbSNP: rs78534766
rs78534766
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs78534766
rs78534766
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
Digestive System Diseases 0.700 1.000 1 2017 2017