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: rs190323149
rs190323149
MIR145 ; CARMN
1.000 0.080 5 149430704 mature miRNA variant C/T snv 4.1E-06
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2019 2019
dbSNP: rs353291
rs353291
MIR145 ; CARMN
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2019 2019
dbSNP: rs353291
rs353291
MIR145 ; CARMN
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2019 2019
dbSNP: rs353291
rs353291
MIR145 ; CARMN
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs353291
rs353291
MIR145 ; CARMN
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2015 2015
dbSNP: rs353291
rs353291
MIR145 ; CARMN
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2020 2020
dbSNP: rs353291
rs353291
MIR145 ; CARMN
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2020 2020
dbSNP: rs41291957
rs41291957
MIR143 ; MIR145 ; CARMN
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2014 2014
dbSNP: rs41291957
rs41291957
MIR143 ; MIR145 ; CARMN
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		0.010 1.000 1 2013 2013
dbSNP: rs41291957
rs41291957
MIR143 ; MIR145 ; CARMN
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs41291957
rs41291957
MIR143 ; MIR145 ; CARMN
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.010 1.000 1 2019 2019
dbSNP: rs41291957
rs41291957
MIR143 ; MIR145 ; CARMN
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2013 2013
dbSNP: rs41291957
rs41291957
MIR143 ; MIR145 ; CARMN
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2014 2014
dbSNP: rs41291957
rs41291957
MIR143 ; MIR145 ; CARMN
0.882 0.200 5 149428827 intron variant G/A snv 0.12
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease 		0.010 1.000 1 2014 2014
dbSNP: rs74693964
rs74693964
MIR145 ; CARMN
1.000 0.080 5 149430798 intron variant C/T snv 8.8E-04
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2018 2018