rs1897478

This is a intron variant variant in the MIR217HG gene.

GWAS Catalog Trait Associations (3)

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

Inguinal hernia

Allele T
OR 1.13
p 5.0e-27
N 275,546
Major Consortium StudyLarge GWAS
European

pulse pressure measurement

Allele T
OR 0.15
p 5.0e-17
N 1,028,980
Large GWAS
multi-ancestry

systolic blood pressure

Allele T
OR 0.16
p 2.0e-10
N 1,028,980
Large GWAS
multi-ancestry

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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