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: rs1834481
rs1834481
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.010 1.000 1 2008 2008
dbSNP: rs1834481
rs1834481
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer
0.010 1.000 1 2008 2008
dbSNP: rs1834481
rs1834481
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
0.010 1.000 1 2015 2015
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0005411
Disease: Biliary Atresia
Biliary Atresia
0.010 1.000 1 2018 2018
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2013 2013
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2011 2011
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.010 1.000 1 2015 2015
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0009319
Disease: Colitis
Colitis
0.010 1.000 1 2019 2019
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
0.010 1.000 1 2013 2013
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0031099
Disease: Periodontitis
Periodontitis
0.010 1.000 1 2017 2017
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
0.010 1.000 1 2017 2017
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
0.010 1.000 1 2018 2018
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases
0.010 1.000 1 2016 2016
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0010823
Disease: Cytomegalovirus Infections
Cytomegalovirus Infections
0.010 1.000 1 2019 2019
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 1.000 1 2010 2010
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C3843756
Disease: Ulcerative colitis or Crohn's
Ulcerative colitis or Crohn's
0.010 1.000 1 2019 2019
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2016 2016
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.010 1.000 1 2019 2019
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm
0.010 1.000 1 2018 2018
dbSNP: rs187238
rs187238
0.602 0.680 11 112164265 intron variant C/A;G snv
Congenital atresia of extrahepatic bile duct
0.010 1.000 1 2018 2018