ClinVar Miner

List of variants in gene RHOBTB2 reported by NIHR Bioresource Rare Diseases, University of Cambridge

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_015178.3(RHOBTB2):c.1466G>A (p.Arg489Gln)	rs1554504684

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