KCNE2 and Hereditary Thrombocytopenia And Hematological Cancer Predisposition Syndrome Associated With Runx1: Association Evidence

At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Provenance

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

KCNE2

2 source summaries

A gene summary alongside the source descriptions it was distilled from.

Hereditary Thrombocytopenia And Hematological Cancer Predisposition Syndrome Associated With Runx1

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Population genetics

1 GWAS phenotype

Gene-associated GWAS phenotypes matching the disorder, with best SNP, score, risk-allele frequency and effect size.

Literature

5 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

Provenance

9 references

Every source and publication cited across this dossier, as one numbered reference list.