List of variants in gene RHOBTB2 reported as pathogenic by Institute Of Human Genetics Munich, Klinikum Rechts Der Isar, Tu München

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_015178.3(RHOBTB2):c.1382G>A (p.Arg461His)	rs1554504663
NM_015178.3(RHOBTB2):c.1453C>T (p.Arg485Cys)	rs1563292586
NM_015178.3(RHOBTB2):c.1465C>T (p.Arg489Trp)	rs1554504681
NM_015178.3(RHOBTB2):c.1466G>A (p.Arg489Gln)	rs1554504684

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