List of variants in gene combination FZD4, PRSS23 reported as uncertain significance by GeneDx

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_012193.4(FZD4):c.766A>G (p.Ile256Val)	rs104894223	0.00054
NM_012193.4(FZD4):c.457G>A (p.Asp153Asn)	rs118039628	0.00010
NM_012193.4(FZD4):c.829C>T (p.Arg277Trp)	rs768216168	0.00010
NM_012193.4(FZD4):c.904T>A (p.Cys302Ser)	rs1447260910	0.00001
NM_012193.4(FZD4):c.1345A>G (p.Thr449Ala)
NM_012193.4(FZD4):c.1567G>C (p.Gly523Arg)	rs199577384
NM_012193.4(FZD4):c.571T>C (p.Tyr191His)	rs2495868415
NM_012193.4(FZD4):c.976A>C (p.Thr326Pro)

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