rs509360, MYRF;TMEM258

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.
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 11 61781087 intron variant A/G snv 0.61 0.52 0.700 1.000 1 2011 2011
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 11 61781087 intron variant A/G snv 0.61 0.52 0.700 1.000 1 2018 2018
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 11 61781087 intron variant A/G snv 0.61 0.52 0.700 1.000 1 2012 2012