List of variants in gene PEX19 reported as likely benign by Eurofins NTD LLC (GA)

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002857.4(PEX19):c.261C>T (p.Phe87=)	rs146644725	0.00206
NM_002857.4(PEX19):c.459G>A (p.Leu153=)	rs78340311	0.00098
NM_002857.4(PEX19):c.16G>A (p.Glu6Lys)	rs145845197	0.00093
NM_002857.4(PEX19):c.30C>T (p.Val10=)	rs144440223
NM_002857.4(PEX19):c.726C>T (p.Thr242=)	rs564013133

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