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: rs174551
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 4 2018 2019
dbSNP: rs174551
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 3 2015 2019
dbSNP: rs174551
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2018 2019
dbSNP: rs174551
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2018 2019
dbSNP: rs174559
rs174559
FADS1 ; FADS2
11 61814184 non coding transcript exon variant G/A snv 0.23
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 2 2017 2019
dbSNP: rs174559
rs174559
FADS1 ; FADS2
11 61814184 non coding transcript exon variant G/A snv 0.23
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 2 2017 2019
dbSNP: rs174544
rs174544
FADS1 ; FADS2
11 61800281 3 prime UTR variant C/A snv 0.25
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs174551
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs174551
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs174555
rs174555
FADS1 ; FADS2
11 61812288 intron variant T/C snv 0.26
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs174555
rs174555
FADS1 ; FADS2
11 61812288 intron variant T/C snv 0.26
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs174555
rs174555
FADS1 ; FADS2
11 61812288 intron variant T/C snv 0.26
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs174565
rs174565
FADS1 ; FADS2
11 61824164 intron variant C/G snv 0.15
CUI: C0043094
Disease: Weight Gain
Weight Gain 		0.700 1.000 1 2019 2019
dbSNP: rs61897795
rs61897795
FADS2
11 61850697 intron variant A/G snv 9.5E-02
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs61897795
rs61897795
FADS2
11 61850697 intron variant A/G snv 9.5E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs77466626
rs77466626
FADS2
11 61864218 3 prime UTR variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 1.000 1 2014 2019
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 1 2012 2012
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2015 2015
dbSNP: rs4246215
rs4246215
FEN1 ; FADS2
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2019 2019