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: rs243866
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle 		0.010 1.000 1 2010 2010
dbSNP: rs243866
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19
CUI: C0275544
Disease: Congenital infectious disease
Congenital infectious disease 		0.010 1.000 1 2016 2016
dbSNP: rs243866
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19
CUI: C0745130
Disease: Resistant hypertensive disorder
Resistant hypertensive disorder 		0.010 1.000 1 2017 2017
dbSNP: rs243866
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.010 1.000 1 2009 2009
dbSNP: rs243866
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		0.010 1.000 1 2013 2013
dbSNP: rs243866
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.010 1.000 1 2017 2017
dbSNP: rs243866
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2019 2019
dbSNP: rs243866
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2012 2012