List of variants reported as likely benign for Peroxisome biogenesis disorder 7A by Illumina Clinical Services Laboratory,Illumina

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Total variants: 12

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HGVS	dbSNP
NM_001127649.3(PEX26):c.*114C>T	rs45500699
NM_001127649.3(PEX26):c.*1740C>G	rs139987168
NM_001127649.3(PEX26):c.*2162G>A	rs45489191
NM_001127649.3(PEX26):c.*2311G>T	rs74714634
NM_001127649.3(PEX26):c.*2703G>A	rs0
NM_001127649.3(PEX26):c.*279G>A	rs0
NM_001127649.3(PEX26):c.*566T>C	rs0
NM_001127649.3(PEX26):c.*925A>G	rs115277831
NM_001127649.3(PEX26):c.-363G>C	rs138787474
NM_001127649.3(PEX26):c.130C>T (p.Leu44Phe)	rs150895887
NM_001127649.3(PEX26):c.457C>G (p.Leu153Val)	rs12484657
NM_001127649.3(PEX26):c.815-13C>T	rs139370593

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