List of variants reported as uncertain significance for rickets by FAHD UNIT, Department of Genetics, King Faisal Specialist Hospital and Research Centre

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000376.3(VDR):c.803T>C (p.Ile268Thr)	rs1164008328	0.00001
NM_000376.3(VDR):c.2T>G (p.Met1Arg)	rs2228570
NM_000376.3(VDR):c.820C>T (p.Arg274Cys)	rs757881350

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