rs149698
This variant is located in the FTH1;BEST1 gene.
▶GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (3)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
Red cell distribution width
Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.02
p 7.0e-19
N 394,642
Large GWAS
European
lysophosphatidylcholine measurement
Harshfield EL et al. “Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci.” Bmc Medicine 19(1):232 (2021)
Allele A
OR 0.08
p 1.0e-11
N 13,814
Large GWAS
European
lysophosphatidylethanolamine measurement
Harshfield EL et al. “Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci.” Bmc Medicine 19(1):232 (2021)
Allele A
OR 0.07
p 5.0e-11
N 13,814
Large GWAS
European
▶ClinVar annotation
Benign★★★☆
11 submitters2 publicationsnot specified; Vitelliform macular dystrophy 2; Autosomal dominant vitreoretinochoroidopathy; Retinitis Pigmentosa, Recessive; Iron Overload; Retinitis pigmentosa; Autosomal recessive bestrophinopathy; not provided; Retinitis pigmentosa 50; Retinal dystrophy
View on ClinVar →This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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