rs108499, TMEM258;MYRF

N. diseases: 2
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 11 61779765 intron variant C/T snv 0.27 0.700 1.000 2 2012 2013
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 11 61779765 intron variant C/T snv 0.27 0.700 1.000 1 2011 2011