List of variants in gene PEX5 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001351132.2(PEX5):c.1814G>A (p.Ser605Asn)	rs146567534	0.00047
NM_001351132.2(PEX5):c.1522G>A (p.Val508Met)	rs138028549	0.00011
NM_001351132.2(PEX5):c.496C>G (p.Gln166Glu)	rs751043763	0.00011
NM_001351132.2(PEX5):c.1636C>T (p.Arg546Cys)	rs759334733	0.00009
NM_001351132.2(PEX5):c.610A>G (p.Lys204Glu)	rs149289353	0.00009
NM_001351132.2(PEX5):c.1669C>T (p.Arg557Trp)	rs1281539463	0.00001
NM_001351132.2(PEX5):c.78G>C (p.Gln26His)	rs1940818656	0.00001
NM_001351132.2(PEX5):c.147+32_147+121del
NM_001351132.2(PEX5):c.1768C>G (p.Arg590Gly)	rs139347001
NM_001351132.2(PEX5):c.596G>A (p.Ser199Asn)	rs750906889
NM_001351132.2(PEX5):c.901C>G (p.Arg301Gly)	rs767306549

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