rs174594, FADS2

N. diseases: 14
Source: ALL
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
432 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
306 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
374 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
370 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
373 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
1962 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
609 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
425 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
375 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
688 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
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 0.776 0.160 11 61852357 intron variant C/A;T snv 0.700 1.000 1 2019 2019