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: rs7495132
rs7495132
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 2 2012 2017
dbSNP: rs7495132
rs7495132
0.790 0.080 15 90629669 intron variant C/T snv 0.12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
0.790 0.080 15 90629669 intron variant C/T snv 0.12
Malignant neoplasm of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
0.790 0.080 15 90629669 intron variant C/T snv 0.12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
0.790 0.080 15 90629669 intron variant C/T snv 0.12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
0.790 0.080 15 90629669 intron variant C/T snv 0.12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2019 2019