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: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C1840311
Disease: Laryngeal cleft
Laryngeal cleft 		0.010 < 0.001 1 2012 2012
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0041408
Disease: Turner Syndrome
Turner Syndrome 		0.010 < 0.001 1 2015 2015
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0751075
Disease: Cancer of Digestive System
Cancer of Digestive System 		0.010 < 0.001 1 2013 2013
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 < 0.001 1 2011 2011
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0024299
Disease: Lymphoma
Lymphoma 		0.030 0.333 3 2004 2017
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C1332979
Disease: Childhood Lymphoma
Childhood Lymphoma 		0.030 0.333 3 2004 2017
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C1332206
Disease: Adult Lymphoma
Adult Lymphoma 		0.030 0.333 3 2004 2017
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases 		0.020 0.500 2 1997 1999
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.020 0.500 2 2005 2013
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0016412
Disease: Folic Acid Deficiency
Folic Acid Deficiency 		0.020 0.500 2 2015 2015
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.050 0.600 5 1999 2013
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects 		0.090 0.667 9 1997 2018
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.060 0.667 6 2008 2018
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.060 0.667 6 2008 2018
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		0.030 0.667 3 2003 2008
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.030 0.667 3 2007 2018
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.040 0.750 4 2003 2008
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		0.050 0.800 5 1998 2013
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.050 0.800 5 2001 2012
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome 		0.100 0.818 11 2003 2014
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0013080
Disease: Down Syndrome
Down Syndrome 		0.100 0.833 12 2003 2014
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0021364
Disease: Male infertility
Male infertility 		0.060 0.833 6 2006 2017
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.100 0.867 15 2007 2020
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.100 0.867 15 2007 2020
dbSNP: rs1805087
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.080 1.000 8 2001 2019