ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as uncertain significance by Fulgent Genetics

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Total variants: 10
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HGVS dbSNP
NM_002977.3(SCN9A):c.1238T>C (p.Ile413Thr) rs200689195
NM_002977.3(SCN9A):c.1280T>C (p.Leu427Ser) rs192406412
NM_002977.3(SCN9A):c.1604C>T (p.Ser535Leu) rs201354321
NM_002977.3(SCN9A):c.1973G>A (p.Arg658His) rs200374987
NM_002977.3(SCN9A):c.2318C>G (p.Thr773Ser) rs200624920
NM_002977.3(SCN9A):c.3505A>G (p.Asn1169Asp) rs750269576
NM_002977.3(SCN9A):c.4335C>G (p.Ile1445Met) rs1362318488
NM_002977.3(SCN9A):c.4787C>T (p.Thr1596Ile) rs200470541
NM_002977.3(SCN9A):c.5787C>G (p.Asn1929Lys) rs371454107
NM_002977.3(SCN9A):c.5915G>T (p.Ser1972Ile) rs770802841

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