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: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2010 2013
dbSNP: rs174555
rs174555
FADS1 ; FADS2
11 61812288 intron variant T/C snv 0.26
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174556
rs174556
FADS1 ; FADS2
0.925 0.160 11 61813163 intron variant C/T snv 0.26
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs968567
rs968567
FADS1 ; FADS2
0.851 0.240 11 61828092 intron variant C/T snv 0.11
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.810 1.000 2 2009 2019
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.800 1.000 1 2010 2010
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2009 2019
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2009 2009
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.800 1.000 1 2011 2016
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.830 1.000 1 2011 2019
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2009 2019
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.800 1.000 1 2012 2016
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.800 1.000 1 2011 2016
dbSNP: rs174547
rs174547
FADS1 ; FADS2
0.742 0.240 11 61803311 intron variant T/C snv 0.28
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs174553
rs174553
FADS1 ; FADS2
1.000 0.040 11 61807686 intron variant A/G;T snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174554
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174556
rs174556
FADS1 ; FADS2
0.925 0.160 11 61813163 intron variant C/T snv 0.26
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2008 2008
dbSNP: rs174556
rs174556
FADS1 ; FADS2
0.925 0.160 11 61813163 intron variant C/T snv 0.26
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs174562
rs174562
FADS1 ; FADS2
1.000 0.080 11 61817672 intron variant A/G snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174566
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs61897792
rs61897792
FADS1 ; FADS2
11 61819414 intron variant C/T snv 7.1E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs968567
rs968567
FADS1 ; FADS2
0.851 0.240 11 61828092 intron variant C/T snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs968567
rs968567
FADS1 ; FADS2
0.851 0.240 11 61828092 intron variant C/T snv 0.11
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011
dbSNP: rs99780
rs99780
FADS1 ; FADS2
1.000 0.080 11 61829161 intron variant C/T snv 0.38
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174568
rs174568
FADS1 ; FADS2
1.000 0.080 11 61826344 missense variant C/A;T snv 0.37
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174559
rs174559
FADS1 ; FADS2
11 61814184 non coding transcript exon variant G/A snv 0.23
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012