rs174528, TMEM258;MYRF

N. diseases: 5
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 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 0.700 1.000 2 2012 2013
Arachidonic acid measurement
CUI: C2316832
Disease: Arachidonic acid measurement
4 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 0.700 1.000 1 2015 2015
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 0.700 1.000 1 2018 2018
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 0.700 1.000 1 2018 2018
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 0.700 1.000 1 2011 2011