ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as uncertain significance for not specified

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Total variants: 15
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NM_002977.3(SCN9A):c.1150G>A (p.Val384Ile) rs200973534
NM_002977.3(SCN9A):c.1966A>G (p.Lys656Glu) rs775090142
NM_002977.3(SCN9A):c.2159T>A (p.Ile720Lys) rs200945460
NM_002977.3(SCN9A):c.2533A>G (p.Ile845Val) rs1218485798
NM_002977.3(SCN9A):c.2611G>C (p.Val871Leu) rs1553487882
NM_002977.3(SCN9A):c.2987G>A (p.Arg996His) rs188145203
NM_002977.3(SCN9A):c.3238A>G (p.Ile1080Val) rs202212176
NM_002977.3(SCN9A):c.3476T>C (p.Ile1159Thr) rs73019664
NM_002977.3(SCN9A):c.3505A>G (p.Asn1169Asp) rs750269576
NM_002977.3(SCN9A):c.3799C>G (p.Leu1267Val) rs180922748
NM_002977.3(SCN9A):c.4115A>G (p.Lys1372Arg) rs779536952
NM_002977.3(SCN9A):c.4228-3T>C rs773953311
NM_002977.3(SCN9A):c.4997A>T (p.Asp1666Val) rs1553473210
NM_002977.3(SCN9A):c.5678G>A (p.Arg1893His) rs79805025
NM_002977.3(SCN9A):c.5758G>C (p.Asp1920His) rs200410805

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