List of variants in gene combination NOC3L, PLCE1 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_016341.4(PLCE1):c.6446C>T (p.Pro2149Leu)	rs192586920	0.00006
NM_016341.4(PLCE1):c.6757G>A (p.Ala2253Thr)	rs180876175
NM_016341.4(PLCE1):c.6853GAG[1] (p.Glu2286del)	rs771798085

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