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: rs174546
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 6 2009 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: rs174570
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2009 2019
dbSNP: rs174548
rs174548
FADS1 ; FADS2
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 1 2012 2019
dbSNP: rs174601
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 1 2012 2018
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: rs174554
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2018 2019
dbSNP: rs174583
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2018 2019
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2019 2019
dbSNP: rs174549
rs174549
FADS1 ; FADS2
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs174550
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 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 1 2018 2018
dbSNP: rs174566
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2019 2019
dbSNP: rs174568
rs174568
FADS1 ; FADS2
1.000 0.080 11 61826344 missense variant C/A;T snv 0.37
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2019 2019
dbSNP: rs174574
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs174577
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018