Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs174529
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 3 2015 2019
dbSNP: rs174529
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2018 2019
dbSNP: rs174529
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2015 2018
dbSNP: rs174529
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34
CUI: C0700379
Disease: Total iron binding capacity function
Total iron binding capacity function 		0.700 1.000 1 2017 2017
dbSNP: rs174529
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs174529
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34
CUI: C1283048
Disease: Iron binding capacity total measurement
Iron binding capacity total measurement 		0.700 1.000 1 2017 2017