ADIPOR1, adiponectin receptor 1, 51094

N. diseases: 148; N. variants: 8
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: rs3737884
rs3737884 		0.882 0.160 1 202944076 non coding transcript exon variant C/T snv 7.6E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs3737884
rs3737884 		0.882 0.160 1 202944076 non coding transcript exon variant C/T snv 7.6E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs7539542
rs7539542 		0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs7539542
rs7539542 		0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2015 2015
dbSNP: rs7539542
rs7539542 		0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs7539542
rs7539542 		0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58
CUI: C1399793
Disease: skin fold (abnormality)
skin fold (abnormality) 		0.010 1.000 1 2006 2006
dbSNP: rs7539542
rs7539542 		0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2008 2008
dbSNP: rs7539542
rs7539542 		0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 < 0.001 1 2020 2020
dbSNP: rs7539542
rs7539542 		0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs7539542
rs7539542 		0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs1342387
rs1342387 		0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.020 1.000 2 2014 2015
dbSNP: rs1342387
rs1342387 		0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.020 1.000 2 2014 2015
dbSNP: rs1342387
rs1342387 		0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.020 1.000 2 2014 2015
dbSNP: rs12733285
rs12733285 		0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.030 0.667 3 2011 2015
dbSNP: rs1342387
rs1342387 		0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.040 1.000 4 2011 2015