List of variants in gene VDR reported as likely benign for bone disorder

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)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000376.3(VDR):c.*437C>G	rs11574119	0.03464
NM_000376.3(VDR):c.*562A>C	rs3858733	0.03190
NM_000376.3(VDR):c.*2974A>T	rs11574139	0.03175
NM_000376.3(VDR):c.*1281G>A	rs7967673	0.02377
NM_000376.3(VDR):c.*1242A>G	rs7954412	0.02375
NM_000376.3(VDR):c.*2827A>G	rs11574138	0.02365
NM_000376.3(VDR):c.*408T>C	rs112308011	0.01929
NM_000376.3(VDR):c.*2593A>G	rs11168263	0.01497
NM_000376.3(VDR):c.*409G>A	rs11574118	0.01495
NM_000376.3(VDR):c.444C>T (p.Ser148=)	rs2229828	0.00638
NM_000376.3(VDR):c.1206C>A (p.Arg402=)	rs2229829	0.00014
NM_000376.3(VDR):c.162G>A (p.Arg54=)	rs774173372	0.00005
NM_000376.3(VDR):c.219A>G (p.Arg73=)	rs369091846	0.00003
NM_000376.3(VDR):c.897C>T (p.Asp299=)	rs746128447	0.00003

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