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

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Total variants: 12

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HGVS	dbSNP
NM_000444.5(PHEX):c.*218A>C	rs141594056
NM_000444.5(PHEX):c.*361T>C	rs182654518
NM_000444.5(PHEX):c.*388A>G	rs759086924
NM_000444.5(PHEX):c.*48G>A	rs765479131
NM_000444.5(PHEX):c.-108A>G	rs149541983
NM_000444.5(PHEX):c.-33C>T	rs5951494
NM_000444.5(PHEX):c.10G>C (p.Glu4Gln)	rs147859619
NM_000444.5(PHEX):c.118+7G>T	rs534550003
NM_000444.5(PHEX):c.1206A>G (p.Gln402=)	rs151234075
NM_000444.5(PHEX):c.489A>G (p.Ser163=)	rs140231382
NM_000444.5(PHEX):c.537T>A (p.Val179=)	rs137961493
NM_000444.5(PHEX):c.81C>T (p.Val27=)	rs139862893

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