rs174576, FADS2

N. diseases: 14
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.
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 2 2012 2013
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 2 2008 2012
Bipolar Disorder
CUI: C0005586
Disease: Bipolar Disorder
839 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Fasting blood glucose measurement
CUI: C0428568
Disease: Fasting blood glucose measurement
212 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Fasting blood sugar result
CUI: C1261430
Disease: Fasting blood sugar result
113 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2012 2012
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2018 2018
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Serum LDL cholesterol measurement
CUI: C0428474
Disease: Serum LDL cholesterol measurement
555 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.851 0.200 11 61836038 intron variant C/A;T snv 0.700 1.000 1 2012 2012
Borderline Personality Disorder
CUI: C0006012
Disease: Borderline Personality Disorder
82 0.851 0.200 11 61836038 intron variant C/A;T snv 0.010 1.000 1 2018 2018
Bronchopulmonary Dysplasia
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
112 0.851 0.200 11 61836038 intron variant C/A;T snv 0.010 1.000 1 2018 2018