List of variants in gene PEX10 reported as likely pathogenic for not provided

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_002617.4(PEX10):c.193+2T>C
NM_002617.4(PEX10):c.193+2_193+27delinsCCTCACCACACTTGCAGGTGTG
NM_002617.4(PEX10):c.338del (p.Leu113fs)	rs878853044
NM_002617.4(PEX10):c.830T>C (p.Leu277Pro)	rs724160000
NM_002617.4(PEX10):c.912+1G>C	rs1553231739

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