Condition: Anemia
rs1559810905 in
IFIH1 gene and
Anemia
PMID 30965144 2020 An extremely severe case of Aicardi-Goutières syndrome 7 with a novel variant in IFIH1.
rs987710 in
IGLV10-54 gene and
Anemia
PMID 21483845 2011 Genome-wide association study identifies genetic loci associated with iron deficiency.
rs1127354 in
ITPA gene and
Anemia
PMID 20637204 2010 Multivariate analysis demonstrated that age, baseline Hb, baseline platelet count, and rs1127354 were independently associated with severe anemia (Hb <10 g/dL).
rs776035233 in
LCAT gene and
Anemia
PMID 31164121 2019 Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia.