Variant: rs7203560 

    present in Gene: NPRL3
    present in Chromosome: 16
    Position on Chromosome: 134391
    Alleles of this Variant: T/G

rs7203560 in NPRL3 gene and Anemia, Sickle Cell PMID 23406172 2013 Perhaps by independently down-regulating expression of the HBA1/HBA2 genes, variants of the HBA1/HBA2 gene regulatory loci, tagged by rs7203560, reduce haemolysis in sickle cell anaemia.

rs7203560 in NPRL3 gene and Corpuscular Hemoglobin Concentration Mean PMID 23263863 2013 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

PMID 31217584 2019 Genetic analyses of diverse populations improves discovery for complex traits.

rs7203560 in NPRL3 gene and Finding of Mean Corpuscular Hemoglobin PMID 23263863 2013 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

PMID 28453575 2017 Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.

rs7203560 in NPRL3 gene and Hemoglobin measurement PMID 23263863 2013 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

rs7203560 in NPRL3 gene and Mean Corpuscular Volume (result) PMID 23263863 2013 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

PMID 28453575 2017 Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.

rs7203560 in NPRL3 gene and Mean corpuscular hemoglobin concentration determination PMID 23263863 2013 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.

rs7203560 in NPRL3 gene and Red Blood Cell Count measurement PMID 23263863 2013 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.