List of variants in gene combination SCN1A, SCN9A reported as likely benign by Athena Diagnostics Inc

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 7

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HGVS	dbSNP
NM_002977.3(SCN9A):c.1964A>G (p.Lys655Arg)	rs121908919
NM_002977.3(SCN9A):c.2733C>T (p.Arg911=)	rs199653503
NM_002977.3(SCN9A):c.2931C>T (p.Leu977=)	rs201430964
NM_002977.3(SCN9A):c.3328C>T (p.Arg1110Trp)	rs190664764
NM_002977.3(SCN9A):c.4612T>C (p.Trp1538Arg)	rs202084411
NM_002977.3(SCN9A):c.4920C>G (p.Leu1640=)
NM_002977.3(SCN9A):c.5746C>T (p.Leu1916Phe)	rs111558968

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