List of variants in gene RHOBTB2 reported as likely benign for genetic developmental and epileptic encephalopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015178.3(RHOBTB2):c.2129C>T (p.Pro710Leu)	rs146723409	0.00064
NM_015178.3(RHOBTB2):c.713C>T (p.Pro238Leu)	rs1810973688

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