List of variants reported as uncertain significance for Xeroderma pigmentosum, group C by Counsyl

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		ClinVar version:

Total variants: 31

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HGVS	dbSNP	gnomAD frequency
NM_004628.5(XPC):c.*156G>A	rs121965092	0.00006
NM_004628.5(XPC):c.2633C>G (p.Ala878Gly)	rs183167499	0.00006
NM_004628.5(XPC):c.2138G>A (p.Arg713His)	rs778769039	0.00005
NM_004628.5(XPC):c.736C>T (p.Pro246Ser)	rs587778761	0.00004
NM_004628.5(XPC):c.2621C>T (p.Pro874Leu)	rs375859472	0.00003
NM_004628.5(XPC):c.597A>C (p.Lys199Asn)	rs587778759	0.00003
NM_004628.5(XPC):c.755A>G (p.Tyr252Cys)	rs587778760	0.00003
NM_004628.5(XPC):c.2722C>T (p.Arg908Ter)	rs199527751	0.00002
NM_004628.5(XPC):c.478G>T (p.Val160Leu)	rs587778763	0.00002
NM_004628.5(XPC):c.718C>T (p.Arg240Cys)	rs552222088	0.00002
NM_004628.5(XPC):c.1229A>G (p.Glu410Gly)	rs587778762	0.00001
NM_004628.5(XPC):c.2011C>T (p.Arg671Cys)	rs771891932	0.00001
NM_004628.5(XPC):c.2033+4C>T	rs753195190	0.00001
NM_004628.5(XPC):c.2537G>C (p.Gly846Ala)	rs55779831	0.00001
NM_004628.5(XPC):c.2703del (p.Ala902fs)	rs1280251289	0.00001
NM_004628.5(XPC):c.1464_1466del (p.Gly489del)	rs1553605750
NM_004628.5(XPC):c.1465_1476del (p.Gly489_Arg492del)	rs1553605733
NM_004628.5(XPC):c.1539G>A (p.Met513Ile)	rs3731130
NM_004628.5(XPC):c.1673_1675dup (p.Cys558dup)	rs1553605670
NM_004628.5(XPC):c.1873-10G>T	rs886058049
NM_004628.5(XPC):c.2033+5G>A	rs374329989
NM_004628.5(XPC):c.2086GTG[3] (p.Val697_Arg698insVal)	rs1423935768
NM_004628.5(XPC):c.2605-2A>T	rs1553604251
NM_004628.5(XPC):c.2633del (p.Ala878fs)	rs1553604236
NM_004628.5(XPC):c.2724AGA[1] (p.Glu909del)	rs751026244
NM_004628.5(XPC):c.2765_2773del (p.Lys922_Lys924del)	rs1553604206
NM_004628.5(XPC):c.2782A>T (p.Lys928Ter)	rs3731177
NM_004628.5(XPC):c.351_352insGTA (p.Thr117_Met118insVal)	rs1358623305
NM_004628.5(XPC):c.52A>C (p.Ser18Arg)	rs587778757
NM_004628.5(XPC):c.621+2dup	rs1553606975
NM_004628.5(XPC):c.90GGA[6] (p.Glu34dup)	rs750450365

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