List of variants reported as pathogenic for Familial encephalopathy with neuroserpin inclusion bodies

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001122752.2(SERPINI1):c.1013A>G (p.His338Arg)	rs121909052
NM_001122752.2(SERPINI1):c.1174G>A (p.Gly392Arg)	rs121909054
NM_001122752.2(SERPINI1):c.1174G>C (p.Gly392Arg)	rs121909054
NM_001122752.2(SERPINI1):c.1175G>A (p.Gly392Glu)	rs121909053
NM_001122752.2(SERPINI1):c.145T>C (p.Ser49Pro)	rs121909051
NM_001122752.2(SERPINI1):c.154A>C (p.Ser52Arg)	rs1577418477

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