rs17367504, MTHFR

N. diseases: 3
Source: GWASDB ×
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.
Blood Pressure
CUI: C0005823
Disease: Blood Pressure
190 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 2 2011 2011
Systolic blood pressure measurement
CUI: C1306620
Disease: Systolic blood pressure measurement
35 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 2 2009 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
388 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 1 2011 2011