Source: ALL

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: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C0027092
Disease: Myopia
Myopia
0.010 1.000 1 2012 2012
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2018 2018
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C0151936
Disease: Disorder of tendon
Disorder of tendon
0.010 1.000 1 2016 2016
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.010 1.000 1 2019 2019
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C1568272
Disease: Tendinopathy
Tendinopathy
0.010 1.000 1 2016 2016
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 1.000 1 2012 2012
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C0025202
Disease: melanoma
melanoma
0.010 1.000 1 2011 2011
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2019 2019
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2019 2019
dbSNP: rs11225395
rs11225395
0.776 0.360 11 102725749 intron variant A/C;G snv
Secondary malignant neoplasm of lymph node
0.010 1.000 1 2007 2007