rs1801621

This variant is located in the BEST1;FTH1 gene.

GWAS Catalog Trait Associations (7)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

fatty acid amount

Allele C
OR
p 3.0e-17
N 239,268
Large GWAS
European

ClinVar annotation

Likely Benign★★★
3 submitters1 publication

Vitelliform macular dystrophy 2; Retinitis Pigmentosa, Recessive; Iron Overload; Autosomal dominant vitreoretinochoroidopathy; Retinitis pigmentosa; not provided

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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