List of variants in gene XPC reported as benign for not specified

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_004628.5(XPC):c.1881T>A (p.Ala627=)	rs2958057	1.00000
NM_004628.5(XPC):c.2605-40A>G	rs2733532	0.65805
NM_004628.5(XPC):c.2251-6A>C	rs2279017	0.64290
NM_004628.5(XPC):c.2604+28C>G	rs2733534	0.41913
NM_004628.5(XPC):c.621+44C>G	rs3729587	0.34174
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.901-22A>G	rs3731125	0.07731
NM_004628.5(XPC):c.1475G>A (p.Arg492His)	rs2227999	0.03986
NM_004628.5(XPC):c.622-16C>G	rs3731111	0.02487
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.1001C>A (p.Pro334His)	rs74737358	0.00806
NM_004628.5(XPC):c.2028C>T (p.Tyr676=)	rs2228004	0.00805
NM_004628.5(XPC):c.860T>G (p.Phe287Cys)	rs35629274	0.00642
NM_004628.5(XPC):c.1443G>T (p.Lys481Asn)	rs182616621	0.00456
NM_004628.5(XPC):c.780-15C>T	rs3731116	0.00344
NM_004628.5(XPC):c.147C>T (p.Ser49=)	rs376018905	0.00005
NM_004628.5(XPC):c.2251-37C>G	rs2470353

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