List of variants reported as uncertain significance for Behr syndrome

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_130837.3(OPA1):c.1311A>G (p.Ile437Met)	rs143319805	0.00056
NM_130837.3(OPA1):c.653C>T (p.Ser218Phe)	rs200243596	0.00022
NM_130837.3(OPA1):c.245A>G (p.Tyr82Cys)	rs749063844	0.00003
NM_130837.3(OPA1):c.2429G>A (p.Arg810His)	rs762258708	0.00001
NM_130837.3(OPA1):c.2617C>T (p.Arg873Trp)	rs143252541	0.00001
NM_130837.3(OPA1):c.861C>G (p.Ile287Met)	rs1732782708	0.00001
NM_130837.3(OPA1):c.113_130del (p.Arg38_Ser43del)	rs863224140
NM_130837.3(OPA1):c.1626A>G (p.Glu542=)	rs1734453026
NM_130837.3(OPA1):c.1811C>T (p.Ser604Leu)	rs1734780550

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