Source: BEFREE

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: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
Familial multiple trichoepitheliomata
0.010 1.000 1 2008 2008
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
0.010 1.000 1 2009 2009
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 < 0.001 1 2011 2011
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.020 1.000 2 2011 2012
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.010 1.000 1 2012 2012
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.030 1.000 3 2008 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.030 1.000 3 2008 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.020 1.000 2 2011 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.020 1.000 2 2011 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0442874
Disease: Neuropathy
Neuropathy
0.010 < 0.001 1 2013 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
0.010 < 0.001 1 2013 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0342942
Disease: Generalized obesity
Generalized obesity
0.010 1.000 1 2013 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C2675519
Disease: Hypoadiponectinemia
Hypoadiponectinemia
0.010 1.000 1 2013 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.010 1.000 1 2013 2013
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.010 1.000 1 2014 2014
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.050 0.800 5 2013 2015
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.050 0.800 5 2013 2015
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 0.750 4 2014 2015
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.030 < 0.001 3 2006 2015
dbSNP: rs1501299
rs1501299
0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.020 1.000 2 2014 2015