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: rs1200746244
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		0.010 1.000 1 2016 2016
dbSNP: rs1200746244
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0236788
Disease: Bipolar II disorder
Bipolar II disorder 		0.010 1.000 1 2015 2015
dbSNP: rs1200746244
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		0.010 1.000 1 2012 2012
dbSNP: rs1200746244
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2012 2012
dbSNP: rs1200746244
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0030193
Disease: Pain
Pain 		0.010 1.000 1 2014 2014
dbSNP: rs1200746244
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		0.010 1.000 1 2012 2012
dbSNP: rs1200746244
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0039494
Disease: Temporomandibular Joint Disorders
Temporomandibular Joint Disorders 		0.010 1.000 1 2014 2014
dbSNP: rs1200746244
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0871189
Disease: Psychotic symptom
Psychotic symptom 		0.010 1.000 1 2012 2012
dbSNP: rs1200746244
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0853193
Disease: Bipolar I disorder
Bipolar I disorder 		0.010 1.000 1 2016 2016
dbSNP: rs142884651
rs142884651
MTHFR ; C1orf167
1.000 0.080 1 11786327 3 prime UTR variant G/A snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2018 2018
dbSNP: rs147257424
rs147257424
MTHFR
0.925 0.080 1 11801299 missense variant C/A;G;T snv 1.2E-05; 1.2E-05
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.010 1.000 1 2016 2016
dbSNP: rs150963282
rs150963282
MTHFR
1.000 0.080 1 11800285 synonymous variant G/T snv 9.9E-05 1.9E-04
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs200100285
rs200100285
MTHFR
0.851 0.080 1 11796313 missense variant T/C;G snv 1.9E-04
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2007 2007
dbSNP: rs200100285
rs200100285
MTHFR
0.851 0.080 1 11796313 missense variant T/C;G snv 1.9E-04
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2007 2007
dbSNP: rs200100285
rs200100285
MTHFR
0.851 0.080 1 11796313 missense variant T/C;G snv 1.9E-04
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2007 2007
dbSNP: rs373524607
rs373524607
MTHFR
1.000 0.080 1 11794397 synonymous variant A/G snv 1.2E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs3737964
rs3737964
CLCN6 ; MTHFR
1.000 0.080 1 11806987 intron variant T/A;C;G snv
CUI: C2745948
Disease: Hyalinosis, Systemic
Hyalinosis, Systemic 		0.010 1.000 1 2019 2019
dbSNP: rs3753584
rs3753584
CLCN6 ; MTHFR
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs3753584
rs3753584
CLCN6 ; MTHFR
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs3753584
rs3753584
CLCN6 ; MTHFR
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		0.010 < 0.001 1 2014 2014
dbSNP: rs3753584
rs3753584
CLCN6 ; MTHFR
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs3753584
rs3753584
CLCN6 ; MTHFR
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 1.000 1 2017 2017
dbSNP: rs4846052
rs4846052
MTHFR
1.000 0.080 1 11797894 intron variant T/A;C snv
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2019 2019
dbSNP: rs746937239
rs746937239
MTHFR
1.000 0.080 1 11801165 synonymous variant C/A snv 4.0E-06
CUI: C0080178
Disease: Spina Bifida
Spina Bifida 		0.010 1.000 1 2013 2013
dbSNP: rs765167328
rs765167328
MTHFR
1.000 0.080 1 11803027 synonymous variant C/T snv 1.6E-05 4.2E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2008 2008