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: C0520909
Disease: Postoperative Nausea and Vomiting
Postoperative Nausea and Vomiting
0.010 1.000 1 2010 2010
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0013421
Disease: Dystonia
Dystonia
0.010 1.000 1 2010 2010
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders
0.010 1.000 1 2010 2010
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
Secondary malignant neoplasm of colon and/or rectum
0.010 1.000 1 2010 2010
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0524528
Disease: Pervasive Development Disorder
Pervasive Development Disorder
0.010 1.000 1 2010 2010
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0237967
Disease: pediatric AIDS
pediatric AIDS
0.010 1.000 1 2010 2010
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder
0.010 < 0.001 1 2010 2010
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0021364
Disease: Male infertility
Male infertility
0.010 1.000 1 2010 2010
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
Human immunodeficiency virus (HIV) II infection category B1
0.020 1.000 2 2006 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C4505072
Disease: Epileptic Syndromes
Epileptic Syndromes
0.020 0.500 2 2009 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
Acute idiopathic thrombocytopenic purpura
0.010 1.000 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus
0.010 1.000 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C1861502
Disease: COLCHICINE RESISTANCE
COLCHICINE RESISTANCE
0.010 1.000 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.010 < 0.001 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C3887898
Disease: Infantile Spasm
Infantile Spasm
0.010 1.000 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0037769
Disease: West Syndrome
West Syndrome
0.010 1.000 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0085695
Disease: Chronic gastritis
Chronic gastritis
0.010 1.000 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms
0.010 1.000 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
0.010 1.000 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma
0.010 < 0.001 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0220597
Disease: Adult Hodgkin Lymphoma
Adult Hodgkin Lymphoma
0.010 < 0.001 1 2011 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.030 1.000 3 2010 2012
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
Precursor Cell Lymphoblastic Leukemia Lymphoma
0.030 1.000 3 2003 2012
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C3266262
Disease: Multiple Chronic Conditions
Multiple Chronic Conditions
0.020 1.000 2 2007 2012