ClinVar Miner

List of variants reported as uncertain significance for rickets by Mendelics

Included ClinVar conditions (21):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_001177316.2(SLC34A3):c.940G>A (p.Ala314Thr)	rs1332288437	0.00001
NM_000376.3(VDR):c.702C>A (p.Val234=)
NM_000444.6(PHEX):c.961G>T (p.Val321Phe)	rs1556025976

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