rs243865, MMP2

N. diseases: 47
Source: BEFREE ×
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.
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
167 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.720 1.000 2 2017 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
861 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.030 0.333 3 2017 2018
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
858 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.030 0.333 3 2017 2018
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
390 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.020 0.500 2 2017 2019
cervical cancer
CUI: C4048328
Disease: cervical cancer
257 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.020 1.000 2 2016 2016
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
266 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.020 1.000 2 2016 2016
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
871 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.020 1.000 2 2018 2019
Intracranial Aneurysm
CUI: C0007766
Disease: Intracranial Aneurysm
93 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.020 1.000 2 2011 2018
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
172 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.020 1.000 2 2017 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.020 1.000 2 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.020 2 2008 2013
Agenesis
CUI: C0000846
Disease: Agenesis
44 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
273 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
278 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
290 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013
Caries (morphologic abnormality)
CUI: C0333519
Disease: Caries (morphologic abnormality)
33 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2012 2012
Cataract
CUI: C0086543
Disease: Cataract
111 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2019 2019
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2019 2019
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2016 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1022 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1 2014 2014
Dental caries
CUI: C0011334
Disease: Dental caries
54 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2012 2012
Dental Fluorosis, Acquired
CUI: C0026618
Disease: Dental Fluorosis, Acquired
10 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2017 2017
Dural Arteriovenous Fistula
CUI: C0752156
Disease: Dural Arteriovenous Fistula
2 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2018 2018
Glaucoma, Open-Angle
CUI: C0017612
Disease: Glaucoma, Open-Angle
32 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2010 2010
Hantavirus Infections
CUI: C0242994
Disease: Hantavirus Infections
10 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2018 2018