rs11225395, MMP8

N. diseases: 11
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2018 2018
Chronic Periodontitis
CUI: C0266929
Disease: Chronic Periodontitis
99 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2012 2012
Disorder of tendon
CUI: C0151936
Disease: Disorder of tendon
14 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2016 2016
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2018 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2019 2019
melanoma
CUI: C0025202
Disease: melanoma
515 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2011 2011
Myopia
CUI: C0027092
Disease: Myopia
167 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2012 2012
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2019 2019
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2007 2007
Tendinopathy
CUI: C1568272
Disease: Tendinopathy
16 0.776 0.360 11 102725749 intron variant A/C;G snv 0.010 1.000 1 2016 2016