ClinVar Miner

List of variants in gene combination PHEX, PTCHD1 reported as likely benign for Familial X-linked hypophosphatemic vitamin D refractory rickets

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP
NM_000444.6(PHEX):c.*48G>A	rs765479131
NM_000444.6(PHEX):c.2068C>A (p.His690Asn)	rs0
NM_000444.6(PHEX):c.2214G>A (p.Thr738=)	rs140742016

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