List of variants reported as likely benign for Xeroderma pigmentosum, group F; XFE progeroid syndrome; Fanconi anemia complementation group Q by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_005236.3(ERCC4):c.2655G>A (p.Thr885=)	rs16963255	0.01026
NM_005236.3(ERCC4):c.2292C>T (p.Ser764=)	rs139406689	0.00060
NM_005236.3(ERCC4):c.1830C>T (p.Tyr610=)	rs763332387	0.00004
NM_005236.3(ERCC4):c.1342G>C (p.Glu448Gln)	rs547209644
NM_005236.3(ERCC4):c.2124C>T (p.Pro708=)	rs376391395
NM_005236.3(ERCC4):c.503C>G (p.Ala168Gly)	rs2020961

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