Neurodevelopmental Disorder with Dysmorphic Facies and Thin Corpus Callosum

Other 5 variants 1 gene

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Associated Genes (1)

SUPT16H

Associated Variants (5)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS2139399670	SUPT16H	—	—	strong
RS2139402444	SUPT16H	—	—	strong
RS2139403510	SUPT16H	—	—	strong
RS2139397506	SUPT16H	—	—	strong
RS2503025907	SUPT16H	—	—	strong