List of variants in gene XPC reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004628.5(XPC):c.1177C>T (p.Arg393Trp)	rs121965090	0.00098
NM_004628.5(XPC):c.2437G>A (p.Val813Ile)	rs371576722	0.00003
NM_004628.5(XPC):c.1952G>A (p.Arg651Gln)	rs374313721	0.00002
NM_004628.5(XPC):c.1345A>G (p.Ser449Gly)	rs185035500	0.00001
NM_004628.5(XPC):c.1955A>C (p.His652Pro)	rs1695908747	0.00001
NM_004628.5(XPC):c.2414A>G (p.His805Arg)	rs1158663983
NM_004628.5(XPC):c.545T>G (p.Ile182Arg)	rs868302213

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