rs9829896 variant

Aliases: KAT2B SNP rs9829896, intronic SNP rs9829896, rs9829896-C, rs9829896-C allele
External links: dbSNP · ClinVar

Evidence from: primary | all sources

Related entities (18)

Subject	Relation	Object	p-value	Evidence
AFR	interacts_with	rs9829896	—	1
EUR	interacts_with	rs9829896	—	1
rs9829896	associated_with	AA	0.05	1
rs9829896	associated_with	AA cohorts	3.93e-10	1
rs9829896	regulates	African American	—	1
rs9829896	associated_with	African American	4.6e-08	2
rs9829896	regulates	CREBBP	0.011	2
rs9829896	associated_with	Dependence symptoms	0.015	1
rs9829896	risk_factor_for	drug dependence	—	1
rs9829896	associated_with	drug dependence	0.0019	1
rs9829896	protective_against	drug dependence	0.12	1
rs9829896	protective_against	drug-seeking behavior	—	1
rs9829896	associated_with	DSM criteria	—	1
rs9829896	associated_with	GAIN	0.0019	1
rs9829896	protective_against	heavy drinking	—	1
rs9829896	associated_with	KAT2B	—	1
rs9829896	regulates	KAT2B	0.05	2
rs9829896	regulates	OPRM1	0.016	2

Mentioned in (1)

Papers in which this entity is mentioned.

KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (2016)

Merged raw entities (5)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.

Raw name	Type	Papers	Mentions
rs9829896	variant	2	13
rs9829896-c	variant	1	5
intronic snp rs9829896	variant	—	—
kat2b snp rs9829896	variant	—	—
rs9829896-c allele	variant	—	—