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: rs876661321
rs876661321
3 186841714 upstream gene variant G/T snv
ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
0.700 0
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
Nervous System Diseases; Cardiovascular Diseases 0.030 < 0.001 3 2006 2015
dbSNP: rs141205818
rs141205818
1.000 0.080 3 186854691 missense variant A/C snv 3.9E-04 1.8E-04
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 < 0.001 2 2010 2014
dbSNP: rs1063539
rs1063539
0.827 0.360 3 186857603 3 prime UTR variant G/A;C snv 0.10
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: rs121917815
rs121917815
0.925 0.120 3 186854303 missense variant C/T snv 4.0E-06; 1.2E-05
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs12495941
rs12495941
0.851 0.280 3 186850391 intron variant G/T snv 0.35
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs138773406
rs138773406
1.000 0.080 3 186854630 missense variant C/A;T snv 2.1E-04; 8.0E-06
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2013 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 < 0.001 1 2015 2015
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0442874
Disease: Neuropathy
Neuropathy
Nervous System Diseases 0.010 < 0.001 1 2013 2013
dbSNP: rs16861194
rs16861194
0.925 0.120 3 186841636 upstream gene variant A/G snv 0.15
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs17300539
rs17300539
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs182052
rs182052
0.701 0.440 3 186842993 intron variant G/A snv 0.38
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs182052
rs182052
0.701 0.440 3 186842993 intron variant G/A snv 0.38
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs2082940
rs2082940
0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv
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: rs2082940
rs2082940
0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 < 0.001 1 2011 2011
dbSNP: rs2082940
rs2082940
0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs2082940
rs2082940
0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
Nutritional and Metabolic Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0206081
Disease: Hyperandrogenism
Hyperandrogenism
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2014 2014
dbSNP: rs2241766
rs2241766
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
Stomatognathic Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs266729
rs266729
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs266729
rs266729
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 < 0.001 1 2015 2015