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: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		0.720 1.000 2 2017 2018
dbSNP: rs142319636
rs142319636
MMP2
0.790 0.080 16 55504828 intron variant A/G snv 3.7E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.710 1.000 1 2016 2016
dbSNP: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.030 0.333 3 2017 2018
dbSNP: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.030 0.333 3 2017 2018
dbSNP: rs17859821
rs17859821
MMP2
1.000 0.040 16 55478141 intron variant G/A;C snv 0.11
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.020 1.000 2 2009 2009
dbSNP: rs2285053
rs2285053
MMP2
0.752 0.320 16 55478465 intron variant C/T snv 0.12
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.020 1.000 2 2007 2019
dbSNP: rs243864
rs243864
MMP2
0.925 0.080 16 55478410 intron variant T/G snv 0.19
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure 		0.020 0.500 2 2009 2009
dbSNP: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.020 0.500 2 2017 2019
dbSNP: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.020 1.000 2 2016 2016
dbSNP: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.020 < 0.001 2 2008 2013
dbSNP: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.020 1.000 2 2016 2016
dbSNP: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.020 1.000 2 2016 2016
dbSNP: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		0.020 1.000 2 2017 2018
dbSNP: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm 		0.020 1.000 2 2011 2018
dbSNP: rs243865
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.020 1.000 2 2018 2019
dbSNP: rs1022088103
rs1022088103
MMP2
16 55485759 missense variant G/A snv
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion 		0.010 1.000 1 2007 2007
dbSNP: rs1132896
rs1132896
MMP2
16 55485623 synonymous variant G/C snv 0.31 0.26
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2018 2018
dbSNP: rs11639960
rs11639960
MMP2
0.925 0.080 16 55499358 intron variant A/G snv 0.26
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 < 0.001 1 2008 2008
dbSNP: rs11639960
rs11639960
MMP2
0.925 0.080 16 55499358 intron variant A/G snv 0.26
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 < 0.001 1 2008 2008
dbSNP: rs11643630
rs11643630
MMP2
0.925 0.080 16 55476547 intron variant T/G snv 0.55
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2009 2009
dbSNP: rs11643630
rs11643630
MMP2
0.925 0.080 16 55476547 intron variant T/G snv 0.55
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs11644561
rs11644561
MMP2
0.925 0.080 16 55475122 intron variant G/A snv 0.20
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2009 2009
dbSNP: rs11644561
rs11644561
MMP2
0.925 0.080 16 55475122 intron variant G/A snv 0.20
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2009 2009
dbSNP: rs11646643
rs11646643
MMP2
1.000 0.040 16 55484965 intron variant A/G snv 0.31
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.010 1.000 1 2015 2015
dbSNP: rs121912955
rs121912955
MMP2
0.925 0.200 16 55491830 missense variant G/A snv
CUI: C0432289
Disease: Winchester syndrome (disorder)
Winchester syndrome (disorder) 		0.010 1.000 1 2005 2005