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: rs16861205
rs16861205
3 186843845 intron variant G/A snv 0.14
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.020 1.000 2 2011 2013
dbSNP: rs16861205
rs16861205
3 186843845 intron variant G/A snv 0.14
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs16861205
rs16861205
3 186843845 intron variant G/A snv 0.14
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs16861209
rs16861209
3 186845325 intron variant C/A;G snv
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2011 2011
dbSNP: rs876661321
rs876661321
3 186841714 upstream gene variant G/T snv
ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 1
0.700 0
dbSNP: rs1259867035
rs1259867035
1.000 0.040 3 186854387 stop gained C/T snv 4.0E-06
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs138227502
rs138227502
0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs138227502
rs138227502
0.925 0.040 3 186853221 missense variant C/T snv 1.8E-04 5.6E-04
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6773957
rs6773957
1.000 0.040 3 186855916 3 prime UTR variant A/C;G snv 0.55
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement
0.800 1.000 1 2009 2009
dbSNP: rs6773957
rs6773957
1.000 0.040 3 186855916 3 prime UTR variant A/C;G snv 0.55
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
Musculoskeletal Diseases 0.010 1.000 1 2018 2018
dbSNP: rs72563732
rs72563732
0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
0.010 1.000 1 2016 2016
dbSNP: rs72563732
rs72563732
0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs72563732
rs72563732
0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04
CUI: C3241937
Disease: Nonalcoholic Steatohepatitis
Nonalcoholic Steatohepatitis
Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs746639990
rs746639990
1.000 0.040 3 186854598 missense variant A/G snv 2.1E-04 7.0E-06
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2018 2018
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: rs1063538
rs1063538
1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2011 2011
dbSNP: rs1063538
rs1063538
1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1063538
rs1063538
1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs1063538
rs1063538
1.000 0.080 3 186856394 3 prime UTR variant T/C snv 0.55
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2011 2011
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: rs1391272583
rs1391272583
0.925 0.080 3 186853177 missense variant T/A snv 4.0E-06
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1391272583
rs1391272583
0.925 0.080 3 186853177 missense variant T/A snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2014 2014
dbSNP: rs201989364
rs201989364
0.882 0.080 3 186854295 missense variant A/G snv 6.4E-05 2.1E-05
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs201989364
rs201989364
0.882 0.080 3 186854295 missense variant A/G snv 6.4E-05 2.1E-05
CUI: C0033860
Disease: Psoriasis
Psoriasis
Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs201989364
rs201989364
0.882 0.080 3 186854295 missense variant A/G snv 6.4E-05 2.1E-05
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2015 2015