rs968567, FADS2;FADS1

N. diseases: 7
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.810 1.000 4 2009 2019
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.700 1.000 1 2016 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.010 1.000 1 2018 2018