ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as likely pathogenic for not provided

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Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_001365536.1(SCN9A):c.902-2A>C rs773824421 0.00005
NM_001365536.1(SCN9A):c.2719C>T (p.Arg907Trp) rs202152511 0.00004
NM_001365536.1(SCN9A):c.4503+1G>T rs746241591 0.00001
NM_001365536.1(SCN9A):c.2600G>A (p.Gly867Asp) rs879254102
NM_001365536.1(SCN9A):c.4507A>T (p.Lys1503Ter) rs876661206
NM_001365536.1(SCN9A):c.4855C>T (p.Arg1619Ter) rs779609081
NM_001365536.1(SCN9A):c.4868T>C (p.Leu1623Pro) rs1131691776
NM_001365536.1(SCN9A):c.4916T>A (p.Met1639Lys) rs2106338008
NM_001365536.1(SCN9A):c.5392G>T (p.Glu1798Ter) rs770416478
NM_001365536.1(SCN9A):c.5569del (p.Asp1857fs) rs1553472910

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