ClinVar Miner

List of variants reported as likely pathogenic for X-linked dominant hypophosphatemic rickets by Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_000444.6(PHEX):c.1875T>G (p.Tyr625Ter) rs1400504292
NM_000444.6(PHEX):c.2140C>T (p.Gln714Ter) rs1569442206

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