RS10895322 Unknown gene

Other Chr 11:102599525

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What This Variant Does

"CLNSIG=1

GWAS Studies (2)

Trait	Risk Allele	OR / Beta	P-value	Study
Neuroblastoma (11q deletion)	G	OR: 2.76	3E-10	PubMed
Shum Visual Learning Test (SVLT) Learning Index (SVLT LI)	G	OR: 0.2	5E-6	PubMed