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: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2018 2018
dbSNP: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
Malignant neoplasm of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.700 1.000 1 2019 2019
dbSNP: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2019 2019
dbSNP: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2019 2019
dbSNP: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2019 2019
dbSNP: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2019 2019
dbSNP: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.700 1.000 1 2019 2019
dbSNP: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
0.700 1.000 1 2019 2019
dbSNP: rs61776719
rs61776719
0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2019 2019