List of variants in gene PEX6 reported as likely benign for not specified

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000287.4(PEX6):c.2426C>T (p.Ala809Val)	rs35830695	0.07353
NM_000287.4(PEX6):c.1646C>T (p.Ala549Val)	rs115960224	0.00687
NM_000287.4(PEX6):c.813G>T (p.Ala271=)	rs35503676	0.00583
NM_000287.4(PEX6):c.882+15_882+16del	rs555409430	0.00189
NM_000287.4(PEX6):c.2436G>A (p.Arg812=)	rs61732156	0.00178
NM_000287.4(PEX6):c.685A>G (p.Arg229Gly)	rs146571927	0.00176
NM_000287.4(PEX6):c.1171G>A (p.Glu391Lys)	rs150046979	0.00175
NM_000287.4(PEX6):c.1491C>T (p.Ser497=)	rs79238506	0.00079
NM_000287.4(PEX6):c.853C>G (p.Pro285Ala)	rs61753220	0.00067
NM_000287.4(PEX6):c.2867C>T (p.Ala956Val)	rs200115671	0.00014
NM_000287.4(PEX6):c.2730G>A (p.Thr910=)	rs774721609	0.00005
NM_000287.4(PEX6):c.804C>T (p.Asp268=)	rs761372470	0.00001
NM_000287.4(PEX6):c.855C>A (p.Pro285=)	rs757897959
NM_000287.4(PEX6):c.969C>T (p.Ile323=)	rs143001881

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