List of variants in gene PEX1 reported as likely benign 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_000466.3(PEX1):c.1360-209G>A	rs6946364	0.03237
NM_000466.3(PEX1):c.2718+134A>G	rs76587269	0.02767
NM_000466.3(PEX1):c.2584-20T>A	rs111535201	0.02687
NM_000466.3(PEX1):c.2088A>G (p.Ile696Met)	rs35996821	0.02553
NM_000466.3(PEX1):c.1671-7T>C	rs74519968	0.01312
NM_000466.3(PEX1):c.1239+161C>G	rs113848550	0.00886
NM_000466.3(PEX1):c.812A>G (p.Asn271Ser)	rs138183109	0.00874
NM_000466.3(PEX1):c.1521G>C (p.Trp507Cys)	rs112822975	0.00803
NM_000466.3(PEX1):c.1484-106A>G	rs200489532	0.00684
NM_000466.3(PEX1):c.1803+185_1803+187del	rs150645900
NM_000466.3(PEX1):c.2226+57del	rs138118520

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