List of variants in gene combination LOC129933826, LOC129933827, LOC129933828, PEX13, PUS10, SANBR reported as pathogenic for autosomal recessive disease

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NC_000002.12:g.60947640_61094952del

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