Source: GWASCAT

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: rs73068325
rs73068325
0.776 0.080 19 58567729 intron variant C/T snv 0.18
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2019 2019
dbSNP: rs73068325
rs73068325
0.776 0.080 19 58567729 intron variant C/T snv 0.18
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2019 2019
dbSNP: rs73068325
rs73068325
0.776 0.080 19 58567729 intron variant C/T snv 0.18
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs73068325
rs73068325
0.776 0.080 19 58567729 intron variant C/T snv 0.18
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs73068325
rs73068325
0.776 0.080 19 58567729 intron variant C/T snv 0.18
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs73068325
rs73068325
0.776 0.080 19 58567729 intron variant C/T snv 0.18
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2019 2019
dbSNP: rs73068325
rs73068325
0.776 0.080 19 58567729 intron variant C/T snv 0.18
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019
dbSNP: rs73068325
rs73068325
0.776 0.080 19 58567729 intron variant C/T snv 0.18
Malignant neoplasm of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs73068325
rs73068325
0.776 0.080 19 58567729 intron variant C/T snv 0.18
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 1 2019 2019
dbSNP: rs73068325
rs73068325
0.776 0.080 19 58567729 intron variant C/T snv 0.18
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2019 2019