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: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.060 1.000 6 2009 2017
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.060 1.000 6 2009 2017
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		0.050 1.000 5 2007 2013
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.040 1.000 4 2011 2018
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.030 1.000 3 2011 2018
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.030 0.667 3 2010 2017
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.020 1.000 2 2007 2018
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.020 1.000 2 2009 2011
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.020 0.500 2 2014 2015
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 1.000 2 2007 2018
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.020 1.000 2 2009 2018
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.020 1.000 2 2009 2018
dbSNP: rs1801157
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.020 1.000 2 2014 2015
dbSNP: rs2297630
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21
CUI: C0398650
Disease: Immune thrombocytopenic purpura
Immune thrombocytopenic purpura 		0.020 1.000 2 2013 2016
dbSNP: rs266085
rs266085
CXCL12
0.851 0.200 10 44378805 intron variant C/T snv 0.32
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.020 1.000 2 2009 2015
dbSNP: rs266085
rs266085
CXCL12
0.851 0.200 10 44378805 intron variant C/T snv 0.32
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.020 1.000 2 2009 2015
dbSNP: rs266085
rs266085
CXCL12
0.851 0.200 10 44378805 intron variant C/T snv 0.32
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.020 1.000 2 2009 2015
dbSNP: rs1029153
rs1029153
CXCL12
1.000 0.080 10 44371698 3 prime UTR variant A/G snv 0.27
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.010 1.000 1 2016 2016
dbSNP: rs1065297
rs1065297
CXCL12
0.925 0.040 10 44370528 3 prime UTR variant A/G snv 5.4E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2018 2018
dbSNP: rs1065297
rs1065297
CXCL12
0.925 0.040 10 44370528 3 prime UTR variant A/G snv 5.4E-02
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.010 1.000 1 2018 2018
dbSNP: rs1065297
rs1065297
CXCL12
0.925 0.040 10 44370528 3 prime UTR variant A/G snv 5.4E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2017 2017
dbSNP: rs10793538
rs10793538
CXCL12
1.000 0.040 10 44381138 intron variant T/A;C snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2017 2017
dbSNP: rs10793538
rs10793538
CXCL12
1.000 0.040 10 44381138 intron variant T/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2018 2018
dbSNP: rs1449295847
rs1449295847
CXCL12
10 44372999 frameshift variant -/G delins
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.010 1.000 1 2014 2014
dbSNP: rs17885289
rs17885289
CXCL12
0.882 0.080 10 44386212 non coding transcript exon variant C/T snv 0.26
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2009 2009