ClinVar Miner

List of variants reported as likely benign for X-linked dominant disease

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_000444.6(PHEX):c.*218A>C rs141594056
NM_000444.6(PHEX):c.*361T>C rs182654518
NM_000444.6(PHEX):c.*388A>G rs759086924
NM_000444.6(PHEX):c.*48G>A rs765479131
NM_000444.6(PHEX):c.-108A>G rs149541983
NM_000444.6(PHEX):c.-33C>T rs5951494
NM_000444.6(PHEX):c.10G>C (p.Glu4Gln) rs147859619
NM_000444.6(PHEX):c.118+7G>T rs534550003
NM_000444.6(PHEX):c.1206A>G (p.Gln402=) rs151234075
NM_000444.6(PHEX):c.489A>G (p.Ser163=) rs140231382
NM_000444.6(PHEX):c.537T>A (p.Val179=) rs137961493
NM_000444.6(PHEX):c.81C>T (p.Val27=) rs139862893

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