ClinVar Miner

List of variants in gene PEX11B reported by Undiagnosed Diseases Network, NIH

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003846.3(PEX11B):c.277C>T (p.Arg93Ter)	rs781939614	0.00004
NM_003846.3(PEX11B):c.595C>T (p.Arg199Ter)	rs781984979	0.00001

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