List of variants in gene EYA4 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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_004100.5(EYA4):c.529G>A (p.Val177Ile)	rs776409783	0.00004
NM_004100.5(EYA4):c.824C>G (p.Ala275Gly)	rs748654006	0.00003
NM_004100.5(EYA4):c.-14A>G	rs760845191	0.00002
NM_004100.5(EYA4):c.1107+10C>G	rs752586864	0.00002
NM_004100.5(EYA4):c.704C>T (p.Pro235Leu)	rs765608642	0.00002
NM_004100.5(EYA4):c.1085C>T (p.Pro362Leu)	rs1168354526	0.00001
NM_004100.5(EYA4):c.438-15T>C	rs752763979	0.00001
NM_004100.5(EYA4):c.438-6A>T	rs1794468804
NM_004100.5(EYA4):c.806A>T (p.Asp269Val)	rs1562457061

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