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: rs2195239
rs2195239
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs2195239
rs2195239
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.010 1.000 1 2019 2019
dbSNP: rs2195239
rs2195239
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs2195239
rs2195239
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2019 2019
dbSNP: rs2195239
rs2195239
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
0.010 1.000 1 2018 2018
dbSNP: rs2195239
rs2195239
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 1.000 1 2012 2012
dbSNP: rs2195239
rs2195239
0.851 0.240 12 102462924 non coding transcript exon variant C/G snv 0.28
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2012 2012
dbSNP: rs2288377
rs2288377
0.925 0.080 12 102480984 intron variant A/G;T snv
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.010 < 0.001 1 2015 2015
dbSNP: rs2288377
rs2288377
0.925 0.080 12 102480984 intron variant A/G;T snv
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.010 1.000 1 2017 2017
dbSNP: rs35767
rs35767
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs35767
rs35767
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2019 2019
dbSNP: rs35767
rs35767
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs35767
rs35767
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
0.010 1.000 1 2017 2017
dbSNP: rs35767
rs35767
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2018 2018
dbSNP: rs35767
rs35767
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv
CUI: C0949059
Disease: Polyp of large intestine
Polyp of large intestine
0.010 1.000 1 2010 2010
dbSNP: rs35767
rs35767
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2018 2018
dbSNP: rs35767
rs35767
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2010 2010
dbSNP: rs4764887
rs4764887
0.925 0.080 12 102430122 intron variant G/A snv 2.2E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs4764887
rs4764887
0.925 0.080 12 102430122 intron variant G/A snv 2.2E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2011 2011
dbSNP: rs5742612
rs5742612
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs5742612
rs5742612
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2017 2017
dbSNP: rs5742612
rs5742612
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2015 2015
dbSNP: rs5742612
rs5742612
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2014 2014
dbSNP: rs5742612
rs5742612
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
0.010 1.000 1 2017 2017
dbSNP: rs5742612
rs5742612
0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.010 1.000 1 2017 2017