List of variants in gene XRCC1 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_006297.3(XRCC1):c.1738C>T (p.Arg580Trp)	rs140655170	0.00006
NM_006297.3(XRCC1):c.209_233dup (p.Glu81fs)
NM_006297.3(XRCC1):c.352C>T (p.Arg118Trp)
NM_006297.3(XRCC1):c.764AGA[1] (p.Lys256del)	rs777476390
NM_006297.3(XRCC1):c.89dup (p.Tyr30Ter)

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