List of variants in gene CYP27B1 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000785.4(CYP27B1):c.1057C>G (p.Pro353Ala)	rs151335249	0.00061
NM_000785.4(CYP27B1):c.40C>T (p.Arg14Cys)	rs150648140	0.00023
NM_000785.4(CYP27B1):c.541G>T (p.Ala181Ser)	rs368126466	0.00019
NM_000785.4(CYP27B1):c.41G>A (p.Arg14His)	rs372223837	0.00004
NM_000785.4(CYP27B1):c.511C>T (p.Arg171Cys)	rs535463729	0.00004
NM_000785.4(CYP27B1):c.454G>A (p.Ala152Thr)	rs777612495
NM_000785.4(CYP27B1):c.974C>T (p.Thr325Met)	rs762118198

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