List of variants in gene RHEB reported as pathogenic

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005614.4(RHEB):c.104A>C (p.Tyr35Ser)	rs1057519950
NM_005614.4(RHEB):c.104A>G (p.Tyr35Cys)	rs1057519950
NM_005614.4(RHEB):c.104_105delinsTA (p.Tyr35Leu)	rs2536111758

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