Source: GWASDB

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: rs11230805
rs11230805
FADS2
11 61835046 intron variant T/C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11539526
rs11539526
FADS2
11 61866298 3 prime UTR variant C/G;T snv 0.15
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12284876
rs12284876
FADS2
11 61846369 intron variant A/G snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs1535
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
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 1 2012 2019
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: 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: 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: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
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: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17156426
rs17156426
FADS2
11 61841851 intron variant A/G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs17156426
rs17156426
FADS2
11 61841851 intron variant A/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17156442
rs17156442
FADS2
11 61846551 intron variant C/T snv 0.11
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs17156442
rs17156442
FADS2
11 61846551 intron variant C/T snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174541
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174541
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs174541
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2011 2011
dbSNP: rs174541
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2011 2011
dbSNP: rs174544
rs174544
FADS1 ; FADS2
11 61800281 3 prime UTR variant C/A snv 0.25
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174545
rs174545
FADS1 ; FADS2
1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174546
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 3 2008 2019
dbSNP: rs174546
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 3 2009 2013