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: rs7539542
rs7539542
0.807 0.200 1 202940846 3 prime UTR variant G/C snv 0.58
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.040 1.000 4 2011 2015
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 0.667 3 2011 2015
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 1.000 2 2014 2015
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 1.000 2 2014 2015
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
Malignant neoplasm of colon and/or rectum
0.020 1.000 2 2014 2015
dbSNP: rs10753929
rs10753929
1.000 0.040 1 202954050 intron variant T/C snv 0.85
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.010 1.000 1 2012 2012
dbSNP: rs10920533
rs10920533
1.000 0.040 1 202956690 intron variant G/A snv 0.22
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2010 2010
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2015 2015
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 < 0.001 1 2012 2012
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2011 2011
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 < 0.001 1 2012 2012
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2015 2015
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs12733285
rs12733285
0.776 0.120 1 202952912 intron variant C/T snv 0.26
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2015 2015
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 < 0.001 1 2012 2012
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2011 2011
dbSNP: rs1342387
rs1342387
0.776 0.120 1 202945228 intron variant T/C snv 0.53
CUI: C0011847
Disease: Diabetes
Diabetes
0.010 < 0.001 1 2012 2012