rs7940310, PAFAH1B2

N. diseases: 3
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.
Soluble Transferrin Receptor Measurement
7 11 117153765 intron variant T/A;C snv 0.800 1.000 1 2013 2013
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 11 117153765 intron variant T/A;C snv 0.700 1.000 1 2013 2013
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 11 117153765 intron variant T/A;C snv 0.700 1.000 1 2012 2012