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: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.100 0.750 32 2005 2018
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.100 0.950 20 2007 2019
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.100 0.850 20 2003 2018
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.100 0.944 18 2007 2017
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C1096063
Disease: Drug Resistant Epilepsy
Drug Resistant Epilepsy
0.100 0.750 16 2007 2017
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.929 14 2003 2019
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.100 0.786 14 2005 2017
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0023530
Disease: Leukopenia
Leukopenia
0.100 0.909 11 2009 2017
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.909 11 2005 2013
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.100 0.800 10 2003 2015
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.100 0.900 10 2005 2013
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
Childhood Acute Lymphoblastic Leukemia
0.100 0.600 10 2003 2017
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0027947
Disease: Neutropenia
Neutropenia
0.080 0.875 8 2009 2017
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
Myeloid Leukemia, Chronic
0.080 0.875 8 2011 2017
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.070 0.714 7 2002 2019
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.060 0.500 6 2004 2016
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.060 0.667 6 2003 2019
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
Malignant neoplasm of colon and/or rectum
0.060 0.833 6 2008 2017
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.060 1.000 6 2004 2014
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.060 0.833 6 2009 2019
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0031069
Disease: Familial Mediterranean Fever
Familial Mediterranean Fever
0.050 1.000 5 2011 2014
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.050 0.800 5 2006 2010
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.050 1.000 5 2006 2019
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
0.050 0.600 5 2002 2014
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0011991
Disease: Diarrhea
Diarrhea
0.050 1.000 5 2009 2017