ClinVar Miner

List of variants in gene RAB34 reported as likely 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_031934.6(RAB34):c.254T>C (p.Ile85Thr)	rs750408092	0.00003
NM_031934.6(RAB34):c.691C>T (p.Arg231Ter)	rs757465924

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