rs174594, FADS2

N. diseases: 13
Source: GWASCAT ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
368 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
97 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
368 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
368 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
368 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
368 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
368 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
236 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Malignant neoplasm of large intestine
CUI: C0346629
Disease: Malignant neoplasm of large intestine
368 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
368 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Phosphatidylinositol measurement
CUI: C0202171
Disease: Phosphatidylinositol measurement
6 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2019 2019
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
550 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2019 2019