rs60176657

This variant is located in the DNAAF3-AS1;DNAAF3;TNNI3 gene.

GWAS Catalog Trait Associations (1)

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

Thrombocytopenia

Allele A
OR 1.28
p 3.0e-18
N 96,432
Large GWAS
East Asian

ClinVar annotation

Likely Benign★★★
6 submitters3 publications

not specified; Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome; Familial restrictive cardiomyopathy; Dilated Cardiomyopathy, Recessive; Hypertrophic cardiomyopathy; not provided; Primary ciliary dyskinesia

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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