Source: CURATED

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: rs7758229
rs7758229
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.810 0.500 1 2011 2013
dbSNP: rs7758229
rs7758229
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.710 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
0.732 0.120 6 160419220 intron variant G/A;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
0.732 0.120 6 160419220 intron variant G/A;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.700 1.000 1 2015 2015
dbSNP: rs7758229
rs7758229
0.732 0.120 6 160419220 intron variant G/A;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
0.732 0.120 6 160419220 intron variant G/A;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
0.732 0.120 6 160419220 intron variant G/A;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2011 2011
dbSNP: rs7758229
rs7758229
0.732 0.120 6 160419220 intron variant G/A;T snv
Malignant neoplasm of large intestine
0.700 1.000 1 2011 2011