List of variants in gene XPC reported as benign by Illumina Laboratory Services, Illumina

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_004628.5(XPC):c.2251-6A>C	rs2279017	0.64290
NM_004628.5(XPC):c.2061G>A (p.Arg687=)	rs2227998	0.26212
NM_004628.5(XPC):c.1496C>T (p.Ala499Val)	rs2228000	0.21224
NM_004628.5(XPC):c.1475G>A (p.Arg492His)	rs2227999	0.03986
NM_004628.5(XPC):c.300G>A (p.Arg100=)	rs2228002	0.02396
NM_004628.5(XPC):c.142C>T (p.Leu48Phe)	rs2229089	0.02177
NM_004628.5(XPC):c.2028C>T (p.Tyr676=)	rs2228004	0.00805
NM_004628.5(XPC):c.1841T>C (p.Phe614Ser)	rs144766677	0.00716
NM_004628.5(XPC):c.860T>G (p.Phe287Cys)	rs35629274	0.00642
NM_004628.5(XPC):c.1734C>A (p.Val578=)	rs3731131	0.00479
NM_004628.5(XPC):c.780-15C>T	rs3731116	0.00344
NM_004628.5(XPC):c.2782A>C (p.Lys928Gln)	rs3731177	0.00285
NM_004628.5(XPC):c.1780C>T (p.Arg594Cys)	rs183238369	0.00126
NM_004628.5(XPC):c.303C>T (p.Asp101=)	rs41545713	0.00095
NM_004628.5(XPC):c.1539G>C (p.Met513Ile)	rs3731130	0.00064

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