List of variants in gene PAX4 reported as benign by PreventionGenetics, part of Exact Sciences

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_001366110.1(PAX4):c.986A>C (p.His329Pro)	rs712701	0.74681
NM_001366110.1(PAX4):c.*211A>G	rs712700	0.74585
NM_001366110.1(PAX4):c.543A>G (p.Gln181=)	rs327517	0.05634
NM_001366110.1(PAX4):c.474C>T (p.Gly158=)	rs77039439	0.04703
NM_001366110.1(PAX4):c.421C>T (p.Arg141Trp)	rs2233578	0.02654
NM_001366110.1(PAX4):c.*190C>T	rs2233585	0.00426
NM_001366110.1(PAX4):c.599G>A (p.Arg200His)	rs2233580	0.00220
NM_001366110.1(PAX4):c.680G>A (p.Arg227Gln)

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