List of variants in gene RFC1 reported as uncertain significance for cerebellar degeneration

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_002913.5(RFC1):c.2014G>A (p.Val672Met)
NM_002913.5(RFC1):c.2936C>T (p.Ala979Val)	rs755911170
NM_002913.5(RFC1):c.398A>G (p.Asn133Ser)	rs1739849007

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