ClinVar Miner

List of variants in gene PEX11B reported as 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)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NC_000001.10:g.(?_145516401)_(145518292_?)del
NM_003846.3(PEX11B):c.108dup (p.Ala37fs)
NM_003846.3(PEX11B):c.63_64del (p.Gln22fs)

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