List of variants reported as likely benign for Familial acute necrotizing encephalopathy by Fulgent Genetics, Fulgent Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_006267.5(RANBP2):c.6609G>A (p.Ala2203=)	rs60199637	0.04502
NM_006267.5(RANBP2):c.1209C>T (p.Ser403=)	rs140275032	0.00951
NM_006267.5(RANBP2):c.1632-16T>C	rs147266881	0.00948
NM_006267.5(RANBP2):c.1087C>T (p.Arg363Cys)	rs149207118	0.00617
NM_006267.5(RANBP2):c.-41G>T	rs372373398	0.00331
NM_006267.5(RANBP2):c.7499C>T (p.Thr2500Ile)	rs140280672	0.00061
NM_006267.5(RANBP2):c.7340C>T (p.Ser2447Phe)	rs200750445	0.00022
NM_006267.5(RANBP2):c.4331C>T (p.Ala1444Val)	rs150309568	0.00002
NM_006267.5(RANBP2):c.7474A>G (p.Thr2492Ala)	rs2693103

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