rs174529, MYRF;TMEM258

N. diseases: 7
Source: INFERRED ×
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
11 61776489 intron variant T/C snv 0.34 0.700 1.000 3 2015 2019
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
11 61776489 intron variant T/C snv 0.34 0.700 1.000 2 2015 2018
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
11 61776489 intron variant T/C snv 0.34 0.700 1.000 2 2018 2019
Iron binding capacity total measurement
CUI: C1283048
Disease: Iron binding capacity total measurement
11 61776489 intron variant T/C snv 0.34 0.700 1.000 1 2017 2017
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
11 61776489 intron variant T/C snv 0.34 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
11 61776489 intron variant T/C snv 0.34 0.700 1.000 1 2018 2018
Total iron binding capacity function
CUI: C0700379
Disease: Total iron binding capacity function
11 61776489 intron variant T/C snv 0.34 0.700 1.000 1 2017 2017