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: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2018 2018
dbSNP: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2018 2018
dbSNP: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 1 2018 2018
dbSNP: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2018 2018
dbSNP: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2018 2018
dbSNP: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2018 2018
dbSNP: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
Malignant neoplasm of large intestine
0.700 1.000 1 2018 2018
dbSNP: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2018 2018
dbSNP: rs17102823
rs17102823
0.776 0.080 14 34894698 intergenic variant A/C;G snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2018 2018