rs17367504, MTHFR

N. diseases: 9
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 5 2009 2018
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 4 2017 2018
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
220 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 2 2011 2011
Mean blood pressure
CUI: C0428886
Disease: Mean blood pressure
344 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 2 2011 2016
Systolic blood pressure measurement
CUI: C1306620
Disease: Systolic blood pressure measurement
95 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 2 2009 2011
Birth Weight
CUI: C0005612
Disease: Birth Weight
369 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 1 2019 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 1 2011 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.030 0.667 3 2011 2017
Hypotension, Orthostatic
CUI: C0020651
Disease: Hypotension, Orthostatic
21 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.010 1.000 1 2012 2012