List of variants in gene VDR reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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.1016T>C (p.Val339Ala)	rs187843998	0.00035
NM_000376.3(VDR):c.889G>A (p.Val297Ile)	rs144756403	0.00014
NM_000376.3(VDR):c.199C>T (p.Arg67Cys)	rs369248365	0.00005
NM_000376.3(VDR):c.14C>T (p.Ala5Val)	rs368441608	0.00004
NM_000376.3(VDR):c.259A>G (p.Ile87Val)	rs387907555	0.00004
NM_000376.3(VDR):c.146+5G>A	rs756376013	0.00003
NM_000376.3(VDR):c.361C>T (p.Arg121Trp)	rs752590757	0.00003
NM_000376.3(VDR):c.519A>T (p.Arg173Ser)	rs199620286	0.00003
NM_000376.3(VDR):c.781G>A (p.Val261Ile)	rs746214307	0.00003
NM_000376.3(VDR):c.1045G>A (p.Ala349Thr)	rs774910763	0.00002
NM_000376.3(VDR):c.257A>G (p.Asp86Gly)	rs534768058	0.00001
NM_000376.3(VDR):c.311G>A (p.Arg104Gln)	rs749763626	0.00001
NM_000376.3(VDR):c.565C>A (p.His189Asn)	rs778063507
NM_000376.3(VDR):c.86A>G (p.Asp29Gly)	rs1280836121

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