List of variants in gene WNT5A 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003392.7(WNT5A):c.448A>G (p.Met150Val)	rs750679240	0.00003
NM_003392.7(WNT5A):c.634G>A (p.Glu212Lys)	rs766388444	0.00003
NM_003392.7(WNT5A):c.937G>A (p.Glu313Lys)	rs369701725	0.00003
NM_003392.7(WNT5A):c.1005C>T (p.Cys335=)	rs762576376	0.00002
NM_003392.7(WNT5A):c.115G>C (p.Val39Leu)	rs1369701937	0.00001
NM_003392.7(WNT5A):c.554A>G (p.Asn185Ser)	rs771010789	0.00001
NM_003392.7(WNT5A):c.-6C>A	rs372156419
NM_003392.7(WNT5A):c.290C>T (p.Ala97Val)	rs2051414784
NM_003392.7(WNT5A):c.685A>G (p.Thr229Ala)	rs886058744

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