rs2954031, None

N. diseases: 9
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 8 125479491 intron variant G/T snv 0.42 0.800 1.000 4 2012 2019
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 8 125479491 intron variant G/T snv 0.42 0.800 1.000 3 2012 2019
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 8 125479491 intron variant G/T snv 0.42 0.800 1.000 2 2012 2018
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 8 125479491 intron variant G/T snv 0.42 0.700 1.000 2 2018 2019
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 8 125479491 intron variant G/T snv 0.42 0.700 1.000 1 2016 2016
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 8 125479491 intron variant G/T snv 0.42 0.700 1.000 1 2016 2016
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 8 125479491 intron variant G/T snv 0.42 0.700 1.000 1 2016 2016
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 8 125479491 intron variant G/T snv 0.42 0.700 1.000 1 2016 2016
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 8 125479491 intron variant G/T snv 0.42 0.700 1.000 1 2012 2012