C0733682[trait identifier] AND "MNM Diagnostics"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 948148	NM_000444.6(PHEX):c.208_212del (p.Val70fs)	PHEX (V70fs)	Microsatellite (frameshift variant)	Familial X-linked hypophosphatemic vitamin D refractory rickets +1 more	GPathogenic
Select item 989452	NC_000023.11:g.22213388_22345581del	CBLL2, PHEX +1 more	Deletion	Familial X-linked hypophosphatemic vitamin D refractory rickets	GPathogenic
Select item 1013602	NC_000023.11:g.22243338_22690207del	CBLL2, LOC126863223 +5 more	Deletion	Familial X-linked hypophosphatemic vitamin D refractory rickets	GPathogenic

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