rs174583, FADS2

N. diseases: 16
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.
Low density lipoprotein cholesterol measurement
1142 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 2 2018 2019
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 2 2012 2013
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 2 2018 2019
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2018 2018
Fasting blood glucose measurement
CUI: C0428568
Disease: Fasting blood glucose measurement
212 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2012 2012
Fasting blood sugar result
CUI: C1261430
Disease: Fasting blood sugar result
113 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2012 2012
High density lipoprotein measurement
1440 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2018 2018
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2018 2018
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011
QT interval feature (observable entity)
226 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2014 2014
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.010 1 2018 2018
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.010 1 2018 2018
Progressive pseudorheumatoid dysplasia
27 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.010 1.000 1 2009 2009
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.010 1 2018 2018