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: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2010 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2012 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2012 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2012 2017
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2010 2010
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 1.000 1 2014 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0523829
Disease: Phosphatidylcholine measurement
Phosphatidylcholine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.700 1.000 1 2018 2018
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2019 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2019 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.700 1.000 1 2018 2018
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015