Random
LoF
Coding
Chip
About

EBF2

See gene in OMIM, GTEx

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FinnGen association results

This table contains for each phenotype the top associated variant in the gene +- 100 kb.

variant	FIN enrichment	phenotype	category	OR	p-value	number of cases	UKBB	UKBB number of cases

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Inguinal hernia

17096 cases, 190557 controls

XI Diseases of the digestive system (K11_)

Loss of function burden

phenotype	variants	p-value	beta	ref/alt cases	ref/alt controls

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All loss of function and missense variants

variant	consequence	info	FIN enrichment	maf	FinnGen phenotypes p < 1E-04	UKBB results

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Drugs targeting EBF2

molecule	type	action	disease	phase	link

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