List of variants reported as uncertain significance for rickets by 3billion

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000376.3(VDR):c.460C>T (p.Arg154Trp)	rs746619116	0.00001
NM_000376.3(VDR):c.1204C>T (p.Arg402Cys)
NM_000444.6(PHEX):c.2040C>A (p.Asn680Lys)	rs1556151526
NM_000444.6(PHEX):c.2248T>G (p.Ter750Glu)
NM_000785.4(CYP27B1):c.1388T>C (p.Leu463Pro)	rs2140396100
NM_001177316.2(SLC34A3):c.1796T>A (p.Leu599Ter)

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