Random
LoF
Coding
Chip
About

CCND2

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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"Type 2 diabetes, definitions combined"

29193 cases, 182573 controls

Diabetes endpoints

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 CCND2

molecule	type	action	disease	phase	link

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