List of variants in gene PEX11B reported as benign for not provided

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_003846.3(PEX11B):c.172+173C>T	rs4471211	0.36173
NM_003846.3(PEX11B):c.375-247G>A	rs12079763	0.08044
NM_003846.3(PEX11B):c.57-82G>A	rs2274612	0.07553
NM_003846.3(PEX11B):c.57-21C>T	rs61731751	0.03739
NM_003846.3(PEX11B):c.483A>G (p.Gly161=)	rs148000769	0.00144
NM_003846.3(PEX11B):c.374+9T>C	rs200094067	0.00004
NM_003846.3(PEX11B):c.458G>A (p.Cys153Tyr)	rs201973197	0.00004
NM_003846.3(PEX11B):c.291C>T (p.Phe97=)	rs151338360	0.00003

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