Disease: Total iron binding capacity function ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs183360145
rs183360145
Entrez Id: 8418;55604
Gene Symbol: CMAHP;CARMIL1
CMAHP;CARMIL1
CUI: C0700379
Disease:
Total iron binding capacity function 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? 28334935 2017