ClinVar Miner

List of variants reported as benign for Peroxisome biogenesis disorder 1B

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000466.3(PEX1):c.2331C>A (p.Gly777=)	rs10278857	0.93013
NM_000466.3(PEX1):c.358-15G>A	rs38809	0.86650
NM_000466.3(PEX1):c.2584-10T>C	rs375129444
NM_000466.3(PEX1):c.2584-10del	rs5885806

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