List of variants reported as likely benign for X-linked dominant disease by Illumina Laboratory Services, Illumina

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000444.6(PHEX):c.537T>A (p.Val179=)	rs137961493	0.00687
NM_000444.6(PHEX):c.10G>C (p.Glu4Gln)	rs147859619	0.00037
NM_000444.6(PHEX):c.2214G>A (p.Thr738=)	rs140742016	0.00035
NM_000444.6(PHEX):c.1483-7T>C	rs369175587	0.00020
NM_000444.6(PHEX):c.631G>A (p.Asp211Asn)	rs370610267	0.00018
NM_000444.6(PHEX):c.2068C>A (p.His690Asn)	rs200733697	0.00017
NM_000444.6(PHEX):c.*48G>A	rs765479131	0.00004
NM_000444.6(PHEX):c.653A>G (p.His218Arg)	rs774907553	0.00003

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