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: rs8099917
rs8099917 		0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.100 0.965 113 2010 2019
dbSNP: rs17782313
rs17782313 		0.683 0.480 18 60183864 intergenic variant T/C snv 0.24
CUI: C0028754
Disease: Obesity
Obesity 		0.900 0.905 41 2008 2019
dbSNP: rs35705950
rs35705950 		0.763 0.240 11 1219991 splice region variant G/A;T snv
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis 		0.900 0.971 33 2011 2019
dbSNP: rs10811661
rs10811661 		0.724 0.400 9 22134095 intergenic variant T/C snv 0.14
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.900 0.955 32 2007 2019
dbSNP: rs2200733
rs2200733 		0.752 0.240 4 110789013 intergenic variant C/T snv 0.18
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.900 0.971 32 2007 2019
dbSNP: rs1111875
rs1111875 		0.776 0.360 10 92703125 intergenic variant C/T snv 0.36
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.900 0.914 25 2007 2020
dbSNP: rs2046210
rs2046210 		0.708 0.280 6 151627231 intergenic variant G/A snv 0.41
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.900 1.000 24 2009 2019
dbSNP: rs2046210
rs2046210 		0.708 0.280 6 151627231 intergenic variant G/A snv 0.41
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.800 1.000 24 2009 2019
dbSNP: rs3851179
rs3851179 		0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.900 0.826 22 2009 2019
dbSNP: rs889312
rs889312 		0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.800 0.958 19 2007 2017
dbSNP: rs12980275
rs12980275 		0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.100 1.000 18 2011 2019
dbSNP: rs889312
rs889312 		0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.800 0.952 18 2007 2017
dbSNP: rs10941679
rs10941679 		0.763 0.120 5 44706396 intergenic variant A/G snv 0.25
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.800 1.000 16 2008 2016
dbSNP: rs10941679
rs10941679 		0.763 0.120 5 44706396 intergenic variant A/G snv 0.25
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.800 1.000 16 2008 2017
dbSNP: rs7923837
rs7923837 		0.882 0.160 10 92722160 intergenic variant G/A;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 0.941 15 2007 2019
dbSNP: rs8099917
rs8099917 		0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff 		0.100 0.933 15 2011 2019
dbSNP: rs10033464
rs10033464 		0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.900 0.933 14 2007 2019
dbSNP: rs12425791
rs12425791 		0.882 0.120 12 674318 downstream gene variant G/A;C snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.100 0.857 14 2009 2019
dbSNP: rs12807809
rs12807809 		0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.900 0.875 14 2009 2019
dbSNP: rs11833579
rs11833579 		0.827 0.200 12 666033 upstream gene variant G/A snv 0.25
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.100 0.846 13 2011 2019
dbSNP: rs12970134
rs12970134 		0.790 0.280 18 60217517 intergenic variant G/A snv 0.21
CUI: C0028754
Disease: Obesity
Obesity 		0.100 0.923 13 2009 2019
dbSNP: rs8099917
rs8099917 		0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		0.900 1.000 13 2009 2019
dbSNP: rs10483727
rs10483727 		0.851 0.040 14 60606157 upstream gene variant T/C snv 0.45
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		0.100 0.917 12 2011 2019
dbSNP: rs2735839
rs2735839 		0.827 0.160 19 50861367 upstream gene variant A/C;G snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.800 0.938 12 2008 2019
dbSNP: rs2735839
rs2735839 		0.827 0.160 19 50861367 upstream gene variant A/C;G snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.800 0.923 12 2008 2019